Canonical Allele Identifier: PA2828327646
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143644
ClinVar Variation Id: 1135970
ClinVar RCV Id: RCV001471449

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Arg118Ser
CA170349
NM_001369394.2:c.354G>C
CA415172926
NM_001369394.2:c.354G>T