Canonical Allele Identifier: PA103660
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 12610
ClinVar RCV Id: RCV000013444 RCV003221783
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Thr58Ile
CA341206
NM_001130442.3:c.173C>T