Canonical Allele Identifier: PA658808172
Gene: DST HGNC NCBI

Linked Data

ClinVar Variation Id: 518376

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138241.1:p.Met3317Ile
CA3867697
NM_001144769.5:c.9951G>A
CA364513898
NM_001144769.5:c.9951G>T
CA364513899
NM_001144769.5:c.9951G>C