Canonical Allele Identifier: PA916047783
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143585

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Phe64Ile
CA274628
NM_001369394.2:c.190T>A