Canonical Allele Identifier: PA2825866638
Gene: DST HGNC NCBI
ClinVar RCV:
RCV001248466
ClinVar Variation:
972435
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138241.1:p.Leu5512Pro
CA3866079
NM_001144769.5:c.16535T>C