Canonical Allele Identifier: PA916047724
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143529
ClinVar RCV Id: RCV000133061

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Trp11Arg
CA270337
NM_001369394.2:c.31T>C
CA415176872
NM_001369394.2:c.31T>A