Canonical Allele Identifier: PA340069
Gene: SRD5A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3339
ClinVar RCV Id: RCV000003503 RCV001269601 RCV001813943
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000339.2:p.Leu55Gln
CA340068
NM_000348.4:c.164T>A