Canonical Allele Identifier: PA2579933352
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1711128
ClinVar RCV Id: RCV002292422
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Asp57Ala
CA378924693
NM_001130442.3:c.170A>C