Canonical Allele Identifier: PA2573197596
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1353033
ClinVar RCV Id: RCV002049617
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Ile396Met
CA3404083
NM_001308122.2:c.1188C>G