ClinGen Allele Registry
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Canonical Allele Identifier:
PA2579936910
Gene: TP53
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-2.371509423
Score
-2.03840047
Score
-0.0486514856
Score
0.4233426964
Score
0.5823978843
Linked Data - NCBI & NCI
ClinVar Allele:
485522
ClinVar RCV:
RCV000581490
RCV001042212
RCV002289864
ClinVar Variation:
492575
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000537.3:p.Gly112Ser
CA397844540
NM_000546.6:c.334G>A