Canonical Allele Identifier: PA658712975
Gene: SRD5A2 HGNC NCBI
ClinVar RCV:
RCV000582093
ClinVar Variation:
492896
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000339.2:p.Glu57Gln
CA1600017
NM_000348.4:c.169G>C