Canonical Allele Identifier: PA2741932915
Gene: SYNGAP1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3007819
ClinVar RCV Id: RCV003864418

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006763.2:p.Met834Ile
CA363625531
NM_006772.3:c.2502G>A
CA363625532
NM_006772.3:c.2502G>C
CA363625535
NM_006772.3:c.2502G>T