Canonical Allele Identifier: PA2828328017
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143630

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Pro106His
CA170340
NM_001369394.2:c.317C>A