Canonical Allele Identifier: PA2826955923
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 36494

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Val207Ile
CA170394
NM_001316337.2:c.619G>A