Canonical Allele Identifier: PA2828325888
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1405732
ClinVar RCV Id: RCV001906666

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Lys14Arg
CA415176830
NM_001369392.2:c.41A>G