Canonical Allele Identifier: PA170357
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143656
ClinVar RCV Id: RCV000133197 RCV002472328 RCV001522685
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Gln239Glu
CA170355
NM_001110792.2:c.715C>G