ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA122552
Gene: HRAS
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
0.429550998
Score
0.0893879198
Score
-0.0680477229
Score
0.1197386252
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000013442
RCV000485616
RCV002272015
ClinVar Variation:
12608
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_005334.1:p.Glu63Lys
CA122551
NM_005343.4:c.187G>A