Canonical Allele Identifier: PA2829419027
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1419240
ClinVar RCV Id: RCV001954653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Thr219Ile
CA360804943
NM_003060.4:c.656C>T