Canonical Allele Identifier: PA916020744
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 379230

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Met201Val
CA3403918
NM_001308122.2:c.601A>G