Canonical Allele Identifier: PA2828327148
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143737

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Pro209Arg
CA270572
NM_001369393.2:c.626C>G