Canonical Allele Identifier: PA916020783
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1424747
ClinVar RCV Id: RCV001924005
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Trp307Arg
CA342662
NM_001308122.2:c.919T>C
CA343116
NM_001308122.2:c.919T>A