Canonical Allele Identifier: PA2826955682
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143609

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Pro80Arg
CA170316
NM_001316337.2:c.239C>G