Canonical Allele Identifier: PA2828328083
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143738

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Pro209Leu
CA270574
NM_001369394.2:c.626C>T