Canonical Allele Identifier: PA2828326848
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3066414
ClinVar RCV Id: RCV003991418

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Pro59Leu
CA415174704
NM_001369393.2:c.176C>T