Canonical Allele Identifier: PA2829600767
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2766820
ClinVar RCV Id: RCV003515930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005334.1:p.Gln43His
CA378924785
NM_005343.4:c.129G>T
CA378924786
NM_005343.4:c.129G>C