Canonical Allele Identifier: PA270537
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Ala291Val
CA270535
NM_001110792.2:c.872C>T