Canonical Allele Identifier: PA645400916
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 280546
ClinVar RCV Id: RCV000314570

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Lys121Glu
CA10603536
NM_001110792.2:c.361A>G