Canonical Allele Identifier: PA2828326769
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2505626

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Arg22His
CA10558640
NM_001369393.2:c.65G>A