Canonical Allele Identifier: PA121716
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 11843
ClinVar RCV Id: RCV000012617 RCV000416315 RCV001090501
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro334Ser
CA121715
NM_001110792.2:c.1000C>T