Canonical Allele Identifier: PA2826955757
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 654994
ClinVar RCV Id: RCV000811076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Gln115Arg
CA415172974
NM_001316337.2:c.344A>G