Canonical Allele Identifier: PA2741856062
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2728772
ClinVar RCV Id: RCV003508676
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Arg251Gly
CA3403947
NM_001308122.2:c.751C>G