Canonical Allele Identifier: PA2829565015
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 3066414
ClinVar RCV Id: RCV003991418

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Pro152Leu
CA415174704
NM_004992.4:c.455C>T