Canonical Allele Identifier: PA2573073289
Gene: DST HGNC NCBI

Linked Data

ClinVar Variation Id: 648459
ClinVar RCV Id: RCV000803193

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361665.1:p.Val7686Met
CA3866057
NM_001374736.1:c.23056G>A