Canonical Allele Identifier: PA2829419096
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 975838
ClinVar RCV Id: RCV001252960

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Met265Arg
CA360805222
NM_003060.4:c.794T>G