Canonical Allele Identifier: PA2829069187
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143761

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373067.1:p.Lys108Arg
CA170424
NM_001386138.1:c.323A>G