Canonical Allele Identifier: PA2829419074
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1440261
ClinVar RCV Id: RCV001936835

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Phe252Leu
CA360805147
NM_003060.4:c.754T>C
CA360805151
NM_003060.4:c.756C>A
CA360805152
NM_003060.4:c.756C>G