Canonical Allele Identifier: PA2828326757
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2499592
ClinVar RCV Id: RCV003223521

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Leu15Pro
CA294701
NM_001369393.2:c.44T>C