Canonical Allele Identifier: PA211934
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 138188
ClinVar RCV Id: RCV000153477 RCV000202489 RCV000224215 RCV000717310 RCV001083234 RCV002498620
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Ala213Val
CA211932
NM_001110792.2:c.638C>T