Canonical Allele Identifier: PA2826924024
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2581708
ClinVar RCV Id: RCV003330484

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Pro16Leu
CA360802271
NM_001308122.2:c.47C>T