Canonical Allele Identifier: PA170265
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143494

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.His64Arg
CA170263
NM_001110792.2:c.191A>G