Canonical Allele Identifier: PA2828326969
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 290402

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356322.1:p.Val114Ala
CA10606762
NM_001369393.2:c.341T>C