Canonical Allele Identifier: PA2826955739
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1301233
ClinVar RCV Id: RCV001733302

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Lys107Thr
CA415173143
NM_001316337.2:c.320A>C