ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2829601025
Gene: HRAS
HGNC
NCBI
Linked Data - Variant Effect Evidence
MaveDb:
Score
-0.120805642
Score
0.1271671907
Score
-0.0376489032
Score
-0.1843628572
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000637303
RCV002358789
ClinVar Variation:
531190
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_005334.1:p.Leu133Phe
CA5779321
NM_005343.4:c.397C>T