Allele Registry

Canonical Allele Identifier: PA096688

Gene: SLC46A1 HGNC NCBI

ClinVar Allele:

34595

ClinVar RCV:

RCV000020948

RCV000059712

ClinVar Variation:

21743

HGVS (amino-acid)	Matching Registered Transcripts
NP_542400.2:p.Pro425Arg	CA026498 NM_080669.6:c.1274C>G