Canonical Allele Identifier: PA658800912
Gene: SRD5A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 529238
ClinVar RCV Id: RCV000634581
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000339.2:p.Ala207Asp
CA1599876
NM_000348.4:c.620C>A