Canonical Allele Identifier: PA2499255233
Gene: DST HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361665.1:p.Leu7655Phe
CA139164585
NM_001374736.1:c.22963C>T