Canonical Allele Identifier: PA2826955811
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 496282

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Ala146Asp
CA415172315
NM_001316337.2:c.437C>A