Canonical Allele Identifier: PA270582
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143742

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Lys316Glu
CA270580
NM_001110792.2:c.946A>G