Canonical Allele Identifier: PA658667209
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 460412
ClinVar RCV Id: RCV000556789

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Phe230Leu
CA127209308
NM_003060.4:c.688T>C
CA360805009
NM_003060.4:c.690C>A
CA360805010
NM_003060.4:c.690C>G