Canonical Allele Identifier: PA916020756
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 6420
ClinVar RCV Id: RCV000006789 RCV000186136 RCV002226443
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Tyr235Cys
CA312941
NM_001308122.2:c.704A>G