Canonical Allele Identifier: PA170306
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143593

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Thr160Ser
CA170305
NM_004992.4:c.479C>G
CA415174438
NM_004992.4:c.478A>T