Canonical Allele Identifier: PA645475103
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 240137
ClinVar RCV Id: RCV000232309
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Thr2Ala
CA10582926
NM_005343.4:c.4A>G