Canonical Allele Identifier: PA2826297718
Gene: SLC46A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 852

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001229295.1:p.Arg113Ser
CA026505
NM_001242366.3:c.337C>A