Canonical Allele Identifier: PA2573078746
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143736

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373068.1:p.Pro79His
CA270570
NM_001386139.1:c.236C>A