Canonical Allele Identifier: PA2826955571
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2687738
ClinVar RCV Id: RCV003484978

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Asn33Ile
CA415176375
NM_001316337.2:c.98A>T