Canonical Allele Identifier: PA2826955593
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143559

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Arg40His
CA274538
NM_001316337.2:c.119G>A