Canonical Allele Identifier: PA916047801
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143609

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Pro80Arg
CA170316
NM_001369394.2:c.239C>G