Canonical Allele Identifier: PA2573197607
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1423237
ClinVar RCV Id: RCV001928693
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Arg424Cys
CA360807727
NM_001308122.2:c.1270C>T