Canonical Allele Identifier: PA2828540900
Gene: DST HGNC NCBI
ClinVar RCV:
RCV001339140
ClinVar Variation:
1036170
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361651.1:p.Gln7621Leu
CA364504761
NM_001374722.1:c.22862A>T