Canonical Allele Identifier: PA2825692520
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2709469
ClinVar RCV Id: RCV003515621
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Gly178Ser
CA378921006
NM_001130442.3:c.532G>A