Canonical Allele Identifier: PA645511159
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 25396
ClinVar RCV Id: RCV000507691

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Ser255Phe
CA342655
NM_001308122.2:c.764C>T