Canonical Allele Identifier: PA099489
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143754

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Pro322Leu
CA270591
NM_004992.4:c.965C>T