Canonical Allele Identifier: PA170315
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143607

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro184Leu
CA170313
NM_001110792.2:c.551C>T