Canonical Allele Identifier: PA2826955529
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 863787
ClinVar RCV Id: RCV001070837

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Gly10Ser
CA415176886
NM_001316337.2:c.28G>A