Canonical Allele Identifier: PA916047733
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 280546
ClinVar RCV Id: RCV000314570

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Lys16Glu
CA10603536
NM_001369394.2:c.46A>G