Canonical Allele Identifier: PA891846033
Gene: SRD5A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 582210
ClinVar RCV Id: RCV000706218
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000339.2:p.Thr120Pro
CA1599955
NM_000348.4:c.358A>C