Canonical Allele Identifier: PA224923
Gene: SRD5A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 97414
ClinVar RCV Id: RCV000083665 RCV001088179 RCV003317085
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000339.2:p.Phe234Leu
CA224922
NM_000348.4:c.702C>G
CA346597822
NM_000348.4:c.702C>A
CA346597828
NM_000348.4:c.700T>C