Allele Registry

Canonical Allele Identifier: PA645459344

Gene: SYP HGNC NCBI

ClinVar Allele:

339363

ClinVar RCV:

RCV000721022

RCV000964094

RCV001821129

ClinVar Variation:

368465

HGVS (amino-acid)	Matching Registered Transcripts
NP_003170.1:p.Gly293Ser	CA10409699 NM_003179.3:c.877G>A