Canonical Allele Identifier: PA2829068827
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143435

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373066.1:p.Ser178Asn
CA170203
NM_001386137.1:c.533G>A