Canonical Allele Identifier: PA2741830569
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2626784
ClinVar RCV Id: RCV003384310

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Glu485Gln
CA10558431
NM_001110792.2:c.1453G>C