Canonical Allele Identifier: PA658802913
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 514291
ClinVar RCV Id: RCV000606190

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Gly15Glu
CA415301126
NM_001110792.2:c.44G>A