Canonical Allele Identifier: PA916047805
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406154

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Pro83Leu
CA16616643
NM_001369394.2:c.248C>T