Canonical Allele Identifier: PA2573242977
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1407404
ClinVar RCV Id: RCV001918427
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Cys184Ser
CA378920918
NM_005343.4:c.551G>C
CA378920926
NM_005343.4:c.550T>A