Canonical Allele Identifier: PA2825868725
Gene: DST HGNC NCBI
ClinVar RCV:
RCV001339140
ClinVar Variation:
1036170
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138242.1:p.Gln5364Leu
CA364504761
NM_001144770.2:c.16091A>T