Canonical Allele Identifier: PA2828545989
Gene: DST HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361663.1:p.Glu7699Ala
CA364503753
NM_001374734.1:c.23096A>C