Canonical Allele Identifier: PA2829065400
Gene: DST HGNC NCBI
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373029.1:p.Asn2933Lys
CA364516422
NM_001386100.1:c.8799T>G
CA364516423
NM_001386100.1:c.8799T>A