Canonical Allele Identifier: PA2826955712
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 156665
ClinVar RCV Id: RCV000144808

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Gly92Ser
CA294704
NM_001316337.2:c.274G>A