Canonical Allele Identifier: PA1139742550
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 988358
ClinVar RCV Id: RCV001269666
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Gly36Glu
CA415175386
NM_001369394.2:c.107G>A