Canonical Allele Identifier: PA2829565007
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2613436
ClinVar RCV Id: RCV003373966

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Thr148Arg
CA415174787
NM_004992.4:c.443C>G