Canonical Allele Identifier: PA199321
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143344

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Val392Met
CA199319
NM_001110792.2:c.1174G>A