Canonical Allele Identifier: PA270409
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_001104262.1:p.Leu150Ser
CA270407
NM_001110792.2:c.449T>C