Canonical Allele Identifier: PA2826955541
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1406613
ClinVar RCV Id: RCV001915903

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Leu15Val
CA415176805
NM_001316337.2:c.43C>G