Canonical Allele Identifier: PA658802936
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 498088
ClinVar RCV Id: RCV000592531

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Gly175Trp
CA415174358
NM_001110792.2:c.523G>T