Canonical Allele Identifier: PA2826297697
Gene: SLC46A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 193481

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229295.1:p.Ala53Val
CA026499
NM_001242366.3:c.158C>T