Canonical Allele Identifier: PA2829069138
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 384750
ClinVar RCV Id: RCV000438431

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373067.1:p.Ile80Val
CA16608767
NM_001386138.1:c.238A>G