Canonical Allele Identifier: PA2828328030
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1537416
ClinVar RCV Id: RCV002157216

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Ser123Gly
CA10558574
NM_001369394.2:c.367A>G