Canonical Allele Identifier: PA2580532826
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1711130
ClinVar RCV Id: RCV002292424
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_789765.1:p.Met67Leu
CA378924639
NM_176795.5:c.199A>T
CA378924640
NM_176795.5:c.199A>C