Canonical Allele Identifier: PA2829832793
Gene: DST HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056363.2:p.Asp5166Asn
CA139162135
NM_015548.5:c.15496G>A