Canonical Allele Identifier: PA222802
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 95190

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Ala439Ser
CA222801
NM_004992.4:c.1315G>T