Canonical Allele Identifier: PA2829565162
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1014197
ClinVar RCV Id: RCV001312900

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Gly231Trp
CA415172510
NM_004992.4:c.691G>T