Canonical Allele Identifier: PA1139695453
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 957604
ClinVar RCV Id: RCV001230608
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Val196Met
CA127208734
NM_001308122.2:c.586G>A