Canonical Allele Identifier: PA658713008
Gene: SRD5A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 492898
ClinVar RCV Id: RCV000581450
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000339.2:p.Tyr91Asp
CA1599995
NM_000348.4:c.271T>G