Canonical Allele Identifier: PA121719
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 11844
ClinVar RCV Id: RCV000012618 RCV000133115 RCV000492792 RCV000991003 RCV000763200 RCV001246099
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro164Ala
CA121717
NM_001110792.2:c.490C>G