Canonical Allele Identifier: PA103532
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 12611
ClinVar RCV Id: RCV000013445 RCV000419902 RCV000436710 RCV000427529 RCV000426668 RCV000436017 RCV000444744
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Ala146Val
CA256494
NM_001130442.3:c.437C>T