Canonical Allele Identifier: PA2580145062
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1923631

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro211Thr
CA10558584
NM_001110792.2:c.631C>A