Canonical Allele Identifier: PA2830416616
Gene: DST HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_899236.1:p.Leu5334Pro
CA3866079
NM_183380.4:c.16001T>C