Canonical Allele Identifier: PA916047747
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 189760

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Asn33Ser
CA280064
NM_001369394.2:c.98A>G