Canonical Allele Identifier: PA2829068416
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 156670

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373066.1:p.Ala11Gly
CA294719
NM_001386137.1:c.32C>G