Canonical Allele Identifier: PA2579930405
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 503536
ClinVar RCV Id: RCV000595459 RCV000681102 RCV000700035
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Arg149Trp
CA378922736
NM_001130442.3:c.445C>T