Canonical Allele Identifier: PA2829069408
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 211454
ClinVar RCV Id: RCV000192988 RCV001521814 RCV002336514 RCV002472371
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373067.1:p.Pro176Ser
CA206184
NM_001386138.1:c.526C>T