Canonical Allele Identifier: PA916047744
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143546

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Val29Met
CA270366
NM_001369394.2:c.85G>A