Canonical Allele Identifier: PA121718
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 11844
ClinVar RCV Id: RCV000012618 RCV000133115 RCV000492792 RCV000991003 RCV000763200 RCV001246099
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Pro152Ala
CA121717
NM_004992.4:c.454C>G