Canonical Allele Identifier: PA2828326952
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 515481
ClinVar RCV Id: RCV000610375 RCV000691182 RCV002528655
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Pro106Arg
CA10558583
NM_001369393.2:c.317C>G