Canonical Allele Identifier: PA270367
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143546

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Val122Met
CA270366
NM_004992.4:c.364G>A