Canonical Allele Identifier: PA2828325948
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2683175
ClinVar RCV Id: RCV003482042

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Lys42Thr
CA415175225
NM_001369392.2:c.125A>C