Canonical Allele Identifier: PA099511
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143562

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Ser134Cys
CA270396
NM_004992.4:c.401C>G