Canonical Allele Identifier: PA2828325266
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Gln134Glu
CA170355
NM_001369391.2:c.400C>G