Canonical Allele Identifier: PA270432
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143583

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Asp168Gly
CA270431
NM_001110792.2:c.503A>G