Allele Registry

Canonical Allele Identifier: PA2828539961

Gene: DST HGNC NCBI

ClinVar RCV:

RCV004018424

ClinVar Variation:

3076107

HGVS (amino-acid)	Matching Registered Transcripts
NP_001361651.1:p.Asn5230Lys	CA364516422 NM_001374722.1:c.15690T>G CA364516423 NM_001374722.1:c.15690T>A