Canonical Allele Identifier: PA170342
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143630
ClinVar RCV Id: RCV000133170 RCV003483519 RCV003638628
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro211His
CA170340
NM_001110792.2:c.632C>A