Canonical Allele Identifier: PA2829564951
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2576682
ClinVar RCV Id: RCV003322987

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Tyr120Cys
CA415176540
NM_004992.4:c.359A>G