Canonical Allele Identifier: PA645459344
Gene: SYP HGNC NCBI

Linked Data

ClinVar Variation Id: 368465

Amino-acid Alleles

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