Canonical Allele Identifier: PA2580112052
Gene: SRD5A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1958711
ClinVar RCV Id: RCV002725597
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000339.2:p.Arg171Ser
CA1599917
NM_000348.4:c.513G>C
CA346598232
NM_000348.4:c.513G>T