Canonical Allele Identifier: PA916020763
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 460412
ClinVar RCV Id: RCV000556789
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Phe254Leu
CA127209308
NM_001308122.2:c.760T>C
CA360805009
NM_001308122.2:c.762C>A
CA360805010
NM_001308122.2:c.762C>G