Allele Registry

Canonical Allele Identifier: PA913201558

Gene: SLC28A1 HGNC NCBI

ClinVar RCV:

RCV000785743

RCV003965581

ClinVar Variation:

634888

HGVS (amino-acid)	Matching Registered Transcripts
NP_001274691.1:p.Arg510Cys	CA7710843 NM_001287762.2:c.1528C>T