Canonical Allele Identifier: PA108362
Gene: SLC22A5 HGNC NCBI
ClinVar RCV:
RCV000006788
ClinVar Variation:
6419
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Pro478Leu
CA340584
NM_003060.4:c.1433C>T