Canonical Allele Identifier: PA2828325014
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 521464
ClinVar RCV Id: RCV000624621

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Trp11Cys
CA415176854
NM_001369391.2:c.33G>T
CA415176857
NM_001369391.2:c.33G>C