Canonical Allele Identifier: PA2829068996
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2504890
ClinVar RCV Id: RCV003234481
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373067.1:p.Gly8Ala
CA415172504
NM_001386138.1:c.23G>C