Canonical Allele Identifier: PA2830416607
Gene: DST HGNC NCBI
ClinVar RCV:
RCV001339140
ClinVar Variation:
1036170
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_899236.1:p.Gln5324Leu
CA364504761
NM_183380.4:c.15971A>T