Canonical Allele Identifier: PA148321
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 95198
ClinVar RCV Id: RCV000081206 RCV000232718 RCV001507027 RCV001079342 RCV002316245 RCV004542785
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Thr215Met
CA148319
NM_001110792.2:c.644C>T