Canonical Allele Identifier: PA916047755
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143559

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Arg40His
CA274538
NM_001369394.2:c.119G>A