Canonical Allele Identifier: PA2573197553
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1449734

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Val250Asp
CA3403946
NM_001308122.2:c.749T>A