Canonical Allele Identifier: PA2828327190
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143754

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Pro229Leu
CA270591
NM_001369393.2:c.686C>T