Canonical Allele Identifier: PA2828326701
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2626784
ClinVar RCV Id: RCV003384310

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Glu380Gln
CA10558431
NM_001369392.2:c.1138G>C