Canonical Allele Identifier: PA2829069851
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143418

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373068.1:p.Pro170Leu
CA232923
NM_001386139.1:c.509C>T