Canonical Allele Identifier: PA2829068410
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 156669
ClinVar Variation Id: 2845786
ClinVar RCV Id: RCV003640178

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373066.1:p.Gly8Arg
CA294716
NM_001386137.1:c.22G>A
CA415172511
NM_001386137.1:c.22G>C