Canonical Allele Identifier: PA2499255231
Gene: DST HGNC NCBI
ClinVar RCV:
RCV001339140
ClinVar Variation:
1036170
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361665.1:p.Gln7645Leu
CA364504761
NM_001374736.1:c.22934A>T