Canonical Allele Identifier: PA170366
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143661
ClinVar RCV Id: RCV000133202 RCV000547951 RCV001689676 RCV004544316 RCV003380481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Gly244Ala
CA170364
NM_001110792.2:c.731G>C