Canonical Allele Identifier: PA233009
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143700
ClinVar RCV Id: RCV000133241 RCV000707260 RCV000766083 RCV001284746 RCV001800457 RCV004019751
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Arg280Trp
CA233007
NM_001110792.2:c.838C>T