Canonical Allele Identifier: PA2580145058
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1716438
ClinVar RCV Id: RCV002304683 RCV003438994
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Ser92Phe
CA415177336
NM_001110792.2:c.275C>T