Canonical Allele Identifier: PA2573078699
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373068.1:p.Gln4Glu
CA170355
NM_001386139.1:c.10C>G