Canonical Allele Identifier: PA2826955943
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143742

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Lys211Glu
CA270580
NM_001316337.2:c.631A>G