Canonical Allele Identifier: PA2580229877
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2135175
ClinVar RCV Id: RCV003048506

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Thr65Arg
CA415174482
NM_001369394.2:c.194C>G