Canonical Allele Identifier: PA2829419519
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 934190
ClinVar RCV Id: RCV001202533

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Pro518Ser
CA360809952
NM_003060.4:c.1552C>T