Canonical Allele Identifier: PA2826955691
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143611

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Pro83Arg
CA170319
NM_001316337.2:c.248C>G