Canonical Allele Identifier: PA2573180157
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1604076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro211Ser
CA415173156
NM_001110792.2:c.631C>T