Canonical Allele Identifier: PA2828325098
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1478558
ClinVar RCV Id: RCV001998645
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Glu50Ala
CA415175004
NM_001369391.2:c.149A>C