Canonical Allele Identifier: PA170342
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143630

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro211His
CA170340
NM_001110792.2:c.632C>A