Canonical Allele Identifier: PA198842
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 188500
ClinVar RCV Id: RCV000168699 RCV000766082 RCV001850385
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Thr350Ser
CA198840
NM_001110792.2:c.1049C>G
CA415168352
NM_001110792.2:c.1048A>T