Canonical Allele Identifier: PA2828325126
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143589
ClinVar Variation Id: 1027605

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Phe64Leu
CA270435
NM_001369391.2:c.192C>G
CA415174547
NM_001369391.2:c.192C>A
CA415174571
NM_001369391.2:c.190T>C