Canonical Allele Identifier: PA170289
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143545
ClinVar RCV Id: RCV000133078 RCV003990984
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Asp133Gly
CA170287
NM_001110792.2:c.398A>G