Canonical Allele Identifier: PA2828326841
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1723812
ClinVar RCV Id: RCV002306373

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Leu57Val
CA415174765
NM_001369393.2:c.169C>G