Canonical Allele Identifier: PA2580195383
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2166280
ClinVar RCV Id: RCV003091678

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Val292Met
CA3403978
NM_001308122.2:c.874G>A