Canonical Allele Identifier: PA2828546013
Gene: DST HGNC NCBI

Linked Data

ClinVar Variation Id: 1051434
ClinVar RCV Id: RCV002548536 RCV001359472
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001361663.1:p.Val7756Met
CA3865990
NM_001374734.1:c.23266G>A