Canonical Allele Identifier: PA270501
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143653

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro237Arg
CA270500
NM_001110792.2:c.710C>G