Canonical Allele Identifier: PA206186
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 211454
ClinVar RCV Id: RCV000192988 RCV001521814 RCV002336514 RCV002472371
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro411Ser
CA206184
NM_001110792.2:c.1231C>T