Allele Registry

Canonical Allele Identifier: PA2826297827

Gene: SLC46A1 HGNC NCBI

ClinVar Allele:

39882

ClinVar RCV:

RCV000023913

RCV000059709

ClinVar Variation:

30925

HGVS (amino-acid)	Matching Registered Transcripts
NP_001229295.1:p.Gly338Arg	CA026494 NM_001242366.3:c.1012G>C