Canonical Allele Identifier: PA096623
Gene: SLC46A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 852

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_542400.2:p.Arg113Ser
CA026505
NM_080669.6:c.337C>A