Canonical Allele Identifier: PA274667
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 156661
ClinVar RCV Id: RCV000144804 RCV000170280
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Met1Leu