Canonical Allele Identifier: PA2828325932
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143556

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356321.1:p.Ala38Asp
CA270384
NM_001369392.2:c.113C>A