Canonical Allele Identifier: PA2828324997
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143520
ClinVar RCV Id: RCV000133051

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Asp4Glu
CA270323
NM_001369391.2:c.12C>A
CA415176991
NM_001369391.2:c.12C>G