Canonical Allele Identifier: PA2825692527
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1422549
ClinVar RCV Id: RCV001919589 RCV002344051 RCV003159220
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Pro179Ser
CA378920992
NM_001130442.3:c.535C>T