Canonical Allele Identifier: PA2826955935
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143738

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Pro209Leu
CA270574
NM_001316337.2:c.626C>T