Canonical Allele Identifier: PA270368
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143546

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Val134Met
CA270366
NM_001110792.2:c.400G>A