Canonical Allele Identifier: PA2579932283
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1692888
ClinVar RCV Id: RCV002259278 RCV003774794
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Thr74Ile
CA378924585
NM_001130442.3:c.221C>T