Canonical Allele Identifier: PA645401768
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 279847

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Glu495Lys
CA10603533
NM_001110792.2:c.1483G>A