Canonical Allele Identifier: PA658713009
Gene: SRD5A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 492899
ClinVar RCV Id: RCV000582682 RCV001821707
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000339.2:p.Tyr91His
CA1599996
NM_000348.4:c.271T>C