Canonical Allele Identifier: PA2828326362
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143309

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Arg251Trp
CA270179
NM_001369392.2:c.751C>T