Canonical Allele Identifier: PA2826955572
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 423593
ClinVar RCV Id: RCV000478123

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Asn33Asp
CA16621247
NM_001316337.2:c.97A>G