Canonical Allele Identifier: PA2825692492
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2820359
ClinVar RCV Id: RCV003627985
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Asn172Lys
CA378921078
NM_001130442.3:c.516C>A
CA378921080
NM_001130442.3:c.516C>G