Canonical Allele Identifier: PA658694969
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 493552
ClinVar RCV Id: RCV000585605 RCV000780398 RCV002065127 RCV004530635
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Ser190Cys
CA10558596
NM_001110792.2:c.569C>G