Canonical Allele Identifier: PA2826955633
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143579

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Pro59Arg
CA270424
NM_001316337.2:c.176C>G