Canonical Allele Identifier: PA2826955731
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1026306
ClinVar RCV Id: RCV001326736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Arg105_Thr110dup
CA10558580
NM_001316337.2:c.313_330dup