Canonical Allele Identifier: PA170252
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143477

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Pro480Ser
CA170251
NM_004992.4:c.1438C>T