Canonical Allele Identifier: PA1139673394
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 851266

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Ala214Gly
CA415173087
NM_001110792.2:c.641C>G