Canonical Allele Identifier: PA658662707
Gene: SRD5A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 459643
ClinVar RCV Id: RCV000553178
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000339.2:p.His232Arg
CA346597847
NM_000348.4:c.695A>G