Canonical Allele Identifier: PA2826144031
Gene: SLC22A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1232453
ClinVar RCV Id: RCV001620273
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171662.1:p.Ile214Phe
CA6059770
NM_001184733.2:c.640A>T