Canonical Allele Identifier: PA2825559237
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1424572
ClinVar RCV Id: RCV001957206
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Asp159Glu
CA10558607
NM_001110792.2:c.477C>G
CA415174859
NM_001110792.2:c.477C>A