Canonical Allele Identifier: PA2579932161
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1198752
ClinVar RCV Id: RCV001563014
ClinVar Variation Id: 1327492
ClinVar RCV Id: RCV001789705

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Phe156Leu
CA378921198
NM_001130442.3:c.468C>G
CA378921199
NM_001130442.3:c.468C>A
CA378921204
NM_001130442.3:c.466T>C