Canonical Allele Identifier: PA2499237973
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1142971

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.His64Gln
CA10558653
NM_001110792.2:c.192C>G
CA415177813
NM_001110792.2:c.192C>A