Canonical Allele Identifier: PA2829069001
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143661

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373067.1:p.Gly9Ala
CA170364
NM_001386138.1:c.26G>C