Canonical Allele Identifier: PA170159
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143317
ClinVar RCV Id: RCV000132841 RCV001465694 RCV003380457 RCV004532589
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Arg366Leu
CA170157
NM_001110792.2:c.1097G>T