Canonical Allele Identifier: PA2829068599
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143761

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373066.1:p.Lys108Arg
CA170424
NM_001386137.1:c.323A>G