Canonical Allele Identifier: PA916047788
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143593
ClinVar RCV Id: RCV000133132 RCV001332544
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Thr67Ser
CA170305
NM_001369394.2:c.200C>G
CA415174438
NM_001369394.2:c.199A>T