Canonical Allele Identifier: PA2828327627
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1026306
ClinVar RCV Id: RCV001326736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Arg105_Thr110dup
CA10558580
NM_001369394.2:c.313_330dup