Canonical Allele Identifier: PA2828327109
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143716

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Ala194Pro
CA270538
NM_001369393.2:c.580G>C