Canonical Allele Identifier: PA2573099212
Gene: SDR9C7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1310088
ClinVar RCV Id: RCV001757156
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_683695.1:p.Ser233Arg
CA385383313
NM_148897.3:c.699C>G
CA385383315
NM_148897.3:c.699C>A
CA385383331
NM_148897.3:c.697A>C