Canonical Allele Identifier: PA2828328157
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143344

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Val287Met
CA199319
NM_001369394.2:c.859G>A