Canonical Allele Identifier: PA270180
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143309

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Arg356Trp
CA270179
NM_001110792.2:c.1066C>T