Canonical Allele Identifier: PA121714
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 11841
ClinVar RCV Id: RCV000012615 RCV000133194
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro237Leu
CA121713
NM_001110792.2:c.710C>T