Canonical Allele Identifier: PA2829066205
Gene: DST HGNC NCBI

Linked Data

ClinVar Variation Id: 648459
ClinVar RCV Id: RCV000803193

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373029.1:p.Val5359Met
CA3866057
NM_001386100.1:c.16075G>A