Canonical Allele Identifier: PA270408
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143567
ClinVar RCV Id: RCV000133101 RCV001508975
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Leu138Ser
CA270407
NM_004992.4:c.413T>C