Canonical Allele Identifier: PA2826955781
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_001303266.1:p.Phe133Leu
CA10581614
NM_001316337.2:c.399T>G
CA415172665
NM_001316337.2:c.399T>A
CA415172685
NM_001316337.2:c.397T>C