Canonical Allele Identifier: PA658807658
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 529846

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Thr264Met
CA3403969
NM_003060.4:c.791C>T