Canonical Allele Identifier: PA2826956359
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 156636
ClinVar RCV Id: RCV000170088 RCV000767162 RCV001048888 RCV002260620 RCV000766080 RCV003162601
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Arg385Gln
CA199452
NM_001316337.2:c.1154G>A