Canonical Allele Identifier: PA274627
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143526

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro113Arg
CA274626
NM_001110792.2:c.338C>G