Canonical Allele Identifier: PA294706
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 156665
ClinVar RCV Id: RCV000144808

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Gly197Ser
CA294704
NM_001110792.2:c.589G>A