Canonical Allele Identifier: PA2828325041
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143543
ClinVar RCV Id: RCV000133076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Tyr27Asp
CA270363
NM_001369391.2:c.79T>G