Canonical Allele Identifier: PA199327
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143749

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Arg321Trp
CA199325
NM_001110792.2:c.961C>T