Canonical Allele Identifier: PA2829069810
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373068.1:p.Pro164Leu
CA170185
NM_001386139.1:c.491C>T