Canonical Allele Identifier: PA2825738213
Gene: SYNGAP1 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001123538.1:p.Lys705Asn
CA363622837
NM_001130066.2:c.2115G>C
CA363622839
NM_001130066.2:c.2115G>T