Canonical Allele Identifier: PA915975059
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 807854
ClinVar RCV Id: RCV000996058

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Lys227Gln
CA415172871
NM_001110792.2:c.679A>C