Allele Registry

Canonical Allele Identifier: PA2825841235

Gene: SPART HGNC NCBI

ClinVar Variation Id: 311764

HGVS (amino-acid)	Matching Registered Transcripts
NP_001135767.1:p.Asp652Asn	CA6949246 NM_001142295.2:c.1954G>A