Canonical Allele Identifier: PA211308
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 95187
ClinVar RCV Id: RCV000081194 RCV000202529 RCV000224642 RCV001081987 RCV000716944 RCV002498425
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Glu409Lys
CA211306
NM_001110792.2:c.1225G>A