Canonical Allele Identifier: PA1139680568
Gene: SRD5A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 973099
ClinVar RCV Id: RCV001249472
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000339.2:p.His162Pro
CA346598294
NM_000348.4:c.485A>C