Allele Registry

Canonical Allele Identifier: PA2741908422

Gene: SLC28A1 HGNC NCBI

ClinVar RCV:

RCV003974663

ClinVar Variation:

3059692

HGVS (amino-acid)	Matching Registered Transcripts
NP_004204.3:p.Val189Ile	CA7710450 NM_004213.5:c.565G>A