Canonical Allele Identifier: PA270423
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143578

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Asp163Gly
CA270421
NM_001110792.2:c.488A>G