Allele Registry

Canonical Allele Identifier: PA2499266182

Gene: SLC28A2 HGNC NCBI

ClinVar RCV:

RCV001681184

ClinVar Variation:

1269551

HGVS (amino-acid)	Matching Registered Transcripts
NP_004203.2:p.Pro22Leu	CA7542055 NM_004212.4:c.65C>T