Canonical Allele Identifier: PA2828326976
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 807855
ClinVar RCV Id: RCV000996059

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Lys117Glu
CA10558576
NM_001369393.2:c.349A>G