Allele Registry

Canonical Allele Identifier: PA645467782

Gene: SLC20A2 HGNC NCBI

ClinVar Variation Id: 363080

HGVS (amino-acid)	Matching Registered Transcripts
NP_006740.1:p.Gly304Ser	CA4733435 NM_006749.5:c.910G>A