Canonical Allele Identifier: PA658802925
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 521464
ClinVar RCV Id: RCV000624621

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Trp116Cys
CA415176854
NM_001110792.2:c.348G>T
CA415176857
NM_001110792.2:c.348G>C