Allele Registry

Canonical Allele Identifier: PA645430393

Gene: SPART HGNC NCBI

ClinVar RCV:

RCV000279728

RCV001850648

RCV004021570

ClinVar Variation:

311764

HGVS (amino-acid)	Matching Registered Transcripts
NP_055902.1:p.Asp652Asn	CA6949246 NM_015087.5:c.1954G>A