Canonical Allele Identifier: PA270397
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143562

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Ser146Cys
CA270396
NM_001110792.2:c.437C>G