Canonical Allele Identifier: PA2826924081
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 193250
ClinVar RCV Id: RCV000173299 RCV000186152 RCV001810432
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001295051.1:p.Pro46Ser
CA312966
NM_001308122.2:c.136C>T