Canonical Allele Identifier: PA2829832722
Gene: DST HGNC NCBI
ClinVar RCV:
RCV001248466
ClinVar Variation:
972435
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056363.2:p.Leu5008Pro
CA3866079
NM_015548.5:c.15023T>C