Canonical Allele Identifier: PA916047770
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143575

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356323.1:p.Asp54Asn
CA170299
NM_001369394.2:c.160G>A