Canonical Allele Identifier: PA2829069198
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 156628

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373067.1:p.Leu113Val
CA294661
NM_001386138.1:c.337C>G