Canonical Allele Identifier: PA2829565097
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1026306
ClinVar RCV Id: RCV001326736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Arg198_Thr203dup
CA10558580
NM_004992.4:c.592_609dup