Canonical Allele Identifier: PA2828327926
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 11831
ClinVar RCV Id: RCV000012604 RCV000132982 RCV001719695 RCV002260597 RCV002371770 RCV004540997
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Gly335Ser
CA121707
NM_001369394.2:c.1003G>A