Canonical Allele Identifier: PA2579932176
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1010014
ClinVar RCV Id: RCV001307584
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Phe90Ser
CA378924377
NM_001130442.3:c.269T>C