Canonical Allele Identifier: PA224913
Gene: SRD5A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97409
ClinVar RCV Id: RCV000083659
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000339.2:p.Gly184Arg
CA224912
NM_000348.4:c.550G>C