Canonical Allele Identifier: PA645510534
Gene: SRD5A2 HGNC NCBI
ClinVar RCV:
RCV000508957
ClinVar Variation:
440485
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000339.2:p.Tyr242Cys
CA346597764
NM_000348.4:c.725A>G