Canonical Allele Identifier: PA2825692523
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 660554
ClinVar RCV Id: RCV000817769
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Gly178Arg
CA378921005
NM_001130442.3:c.532G>C