Canonical Allele Identifier: PA2826955689
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 406154

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Pro83Leu
CA16616643
NM_001316337.2:c.248C>T