Canonical Allele Identifier: PA2826955567
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1506669
ClinVar RCV Id: RCV002006896

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Leu31Val
CA415176431
NM_001316337.2:c.91T>G