Canonical Allele Identifier: PA2579932290
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2840656
ClinVar RCV Id: RCV003628373
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Met67Ile
CA378924633
NM_001130442.3:c.201G>T
CA378924634
NM_001130442.3:c.201G>C
CA378924635
NM_001130442.3:c.201G>A