Canonical Allele Identifier: PA270400
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143563

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Ser146Phe
CA270398
NM_001110792.2:c.437C>T