Canonical Allele Identifier: PA2826956120
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143344

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Val287Met
CA199319
NM_001316337.2:c.859G>A