Canonical Allele Identifier: PA916047729
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 11814
ClinVar RCV Id: RCV000012585 RCV000255874 RCV000552837 RCV001000318 RCV001195924 RCV002247329 RCV002311513 RCV003224092
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Arg13Trp
CA256089
NM_001369394.2:c.37C>T