Canonical Allele Identifier: PA2825692547
Gene: HRAS HGNC NCBI

Linked Data

ClinVar Variation Id: 240138
ClinVar RCV Id: RCV000229010 RCV003993902
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123914.1:p.Met182Ile
CA5779209
NM_001130442.3:c.546G>A
CA378920945
NM_001130442.3:c.546G>T
CA378920946
NM_001130442.3:c.546G>C