Canonical Allele Identifier: PA916047743
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143547

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Val29Ala
CA170290
NM_001369394.2:c.86T>C