Canonical Allele Identifier: PA2826956353
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2626784
ClinVar RCV Id: RCV003384310

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Glu380Gln
CA10558431
NM_001316337.2:c.1138G>C