Canonical Allele Identifier: PA2830416706
Gene: DST HGNC NCBI
ClinVar RCV:
RCV001247638
ClinVar Variation:
971778
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_899236.1:p.Asp5492Asn
CA139162135
NM_183380.4:c.16474G>A