Canonical Allele Identifier: PA2828327162
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143744
ClinVar RCV Id: RCV000133288

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Lys212Glu
CA270583
NM_001369393.2:c.634A>G