Canonical Allele Identifier: PA2829066216
Gene: DST HGNC NCBI
ClinVar RCV:
RCV002023189
ClinVar Variation:
1512748
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373029.1:p.Glu5387Ala
CA364503753
NM_001386100.1:c.16160A>C