Canonical Allele Identifier: PA2829832751
Gene: DST HGNC NCBI
ClinVar RCV:
RCV002023189
ClinVar Variation:
1512748
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_056363.2:p.Glu5067Ala
CA364503753
NM_015548.5:c.15200A>C