Canonical Allele Identifier: PA270338
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143529
ClinVar RCV Id: RCV000133061

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004983.1:p.Trp104Arg
CA270337
NM_004992.4:c.310T>C
CA415176872
NM_004992.4:c.310T>A