Canonical Allele Identifier: PA2499299307
Gene: SLC22A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1283709
ClinVar RCV Id: RCV001691749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_694857.1:p.Met408Val
CA4084017
NM_153187.2:c.1222A>G