Canonical Allele Identifier: PA2829565134
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1678856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Leu213Val
CA10558575
NM_004992.4:c.637C>G