Canonical Allele Identifier: PA2828327648
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1678856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Leu120Val
CA10558575
NM_001369394.2:c.358C>G