Canonical Allele Identifier: PA2828325038
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2445701
ClinVar RCV Id: RCV003155620

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Ala24Gly
CA415176615
NM_001369391.2:c.71C>G