Canonical Allele Identifier: PA2825867867
Gene: DST HGNC NCBI

Linked Data

ClinVar Variation Id: 518376

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138242.1:p.Met3179Ile
CA3867697
NM_001144770.2:c.9537G>A
CA364513898
NM_001144770.2:c.9537G>T
CA364513899
NM_001144770.2:c.9537G>C