Canonical Allele Identifier: PA2826955537
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143533

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Arg13Gly
CA270345
NM_001316337.2:c.37C>G