Canonical Allele Identifier: PA2826955784
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Gln134Glu
CA170355
NM_001316337.2:c.400C>G