Canonical Allele Identifier: PA915975267
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 655951

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro373Ser
CA415168076
NM_001110792.2:c.1117C>T