Canonical Allele Identifier: PA2829068896
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 95190

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373066.1:p.Ala216Ser
CA222801
NM_001386137.1:c.646G>T