Canonical Allele Identifier: PA2579930564
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 578573
ClinVar RCV Id: RCV000701626 RCV003892562
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Asp154Val
CA378921224
NM_001130442.3:c.461A>T