Canonical Allele Identifier: PA2826955645
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143585

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Phe64Ile
CA274628
NM_001316337.2:c.190T>A