Canonical Allele Identifier: PA2830416615
Gene: DST HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_899236.1:p.Leu5334Phe
CA139164585
NM_183380.4:c.16000C>T