Canonical Allele Identifier: PA915975044
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 807855
ClinVar RCV Id: RCV000996059

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Lys222Glu
CA10558576
NM_001110792.2:c.664A>G