Canonical Allele Identifier: PA2828543021
Gene: DST HGNC NCBI
ClinVar RCV:
RCV002023189
ClinVar Variation:
1512748
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361658.1:p.Glu7357Ala
CA364503753
NM_001374729.1:c.22070A>C