Canonical Allele Identifier: PA2828545068
Gene: DST HGNC NCBI
ClinVar RCV:
RCV001339140
ClinVar Variation:
1036170
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361659.1:p.Gln5239Leu
CA364504761
NM_001374730.1:c.15716A>T