Canonical Allele Identifier: PA2829564961
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 423593
ClinVar RCV Id: RCV000478123

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Asn126Asp
CA16621247
NM_004992.4:c.376A>G