Canonical Allele Identifier: PA2829069209
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143309

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373067.1:p.Arg121Trp
CA270179
NM_001386138.1:c.361C>T