Canonical Allele Identifier: PA294697
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 156662
ClinVar RCV Id: RCV000144805
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Glu19Asp
CA294696
NM_001110792.2:c.57G>C
CA415300946
NM_001110792.2:c.57G>T