Canonical Allele Identifier: PA2826955709
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1166038
ClinVar RCV Id: RCV001513735 RCV001724326
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Thr91Ser
CA10558593
NM_001316337.2:c.272C>G
CA415173706
NM_001316337.2:c.271A>T