Canonical Allele Identifier: PA2828328018
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 940151
ClinVar RCV Id: RCV001209680

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Pro106Leu
CA415173153
NM_001369394.2:c.317C>T