Canonical Allele Identifier: PA2829068770
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143383

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373066.1:p.Pro164Leu
CA170185
NM_001386137.1:c.491C>T