Canonical Allele Identifier: PA2573225687
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1412805
ClinVar RCV Id: RCV001943288
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Phe41Leu
CA360802419
NM_003060.4:c.121T>C
CA360802424
NM_003060.4:c.123C>A
CA360802425
NM_003060.4:c.123C>G