Canonical Allele Identifier: PA202771
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 95196
ClinVar RCV Id: RCV000081204 RCV000169946 RCV000815972
ClinVar Variation Id: 393489
ClinVar RCV Id: RCV000445574
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Asp168Glu
CA202769
NM_001110792.2:c.504C>G
CA16609353
NM_001110792.2:c.504C>A