Canonical Allele Identifier: PA2826955588
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 547103

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Arg40Ser
CA415175306
NM_001316337.2:c.118C>A