Canonical Allele Identifier: PA915981697
Gene: DST HGNC NCBI
ClinVar RCV:
RCV000803193
ClinVar Variation:
648459
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138241.1:p.Val5543Met
CA3866057
NM_001144769.5:c.16627G>A