Canonical Allele Identifier: PA294663
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 156628
ClinVar RCV Id: RCV000144771 RCV001800461
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Leu348Val
CA294661
NM_001110792.2:c.1042C>G