Canonical Allele Identifier: PA2829419485
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 836693
ClinVar RCV Id: RCV001037880

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Leu507Phe
CA3404186
NM_003060.4:c.1521G>C
CA360809844
NM_003060.4:c.1521G>T