Canonical Allele Identifier: PA2828325035
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143540
ClinVar RCV Id: RCV000133073

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Gly21Ala
CA270359
NM_001369391.2:c.62G>C