Canonical Allele Identifier: PA915975037
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 654994
ClinVar RCV Id: RCV000811076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Gln220Arg
CA415172974
NM_001110792.2:c.659A>G