Canonical Allele Identifier: PA658662687
Gene: SRD5A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 459638
ClinVar RCV Id: RCV000534325 RCV001269600
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000339.2:p.Asn193Ser
CA1599888
NM_000348.4:c.578A>G