Canonical Allele Identifier: PA1139748330
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 852174
ClinVar RCV Id: RCV001056731 RCV004031788
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.His94Gln
CA378924304
NM_176795.5:c.282C>G
CA378924309
NM_176795.5:c.282C>A