Canonical Allele Identifier: PA645401253
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 236303
ClinVar RCV Id: RCV000225601
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Phe238Leu
CA10581614
NM_001110792.2:c.714T>G
CA415172665
NM_001110792.2:c.714T>A
CA415172685
NM_001110792.2:c.712T>C