Canonical Allele Identifier: PA658695178
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 496282
ClinVar RCV Id: RCV000589763 RCV001175142
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Ala251Asp
CA415172315
NM_001110792.2:c.752C>A