Canonical Allele Identifier: PA2828543063
Gene: DST HGNC NCBI

Linked Data

ClinVar Variation Id: 971778
ClinVar RCV Id: RCV001247638

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361658.1:p.Asp7456Asn
CA139162135
NM_001374729.1:c.22366G>A