Canonical Allele Identifier: PA2826955931
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143734

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Pro209Ala
CA270565
NM_001316337.2:c.625C>G