Canonical Allele Identifier: PA108477
Gene: SLC22A5 HGNC NCBI
ClinVar RCV:
RCV000006792
ClinVar Variation:
6423
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Trp351Arg
CA340586
NM_003060.4:c.1051T>C
CA360806706
NM_003060.4:c.1051T>A