Canonical Allele Identifier: PA2825868761
Gene: DST HGNC NCBI
ClinVar RCV:
RCV002023189
ClinVar Variation:
1512748
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138242.1:p.Glu5433Ala
CA364503753
NM_001144770.2:c.16298A>C