Canonical Allele Identifier: PA916047774
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143579

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Pro59Arg
CA270424
NM_001369394.2:c.176C>G