Canonical Allele Identifier: PA645401378
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 386725
ClinVar RCV Id: RCV000431253 RCV000873957 RCV001519911 RCV003448307 RCV003168669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Ala293Thr
CA10558543
NM_001110792.2:c.877G>A