Canonical Allele Identifier: PA2573180163
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1678856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Leu225Val
CA10558575
NM_001110792.2:c.673C>G