Canonical Allele Identifier: PA270380
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143554

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Gln140Pro
CA270379
NM_001110792.2:c.419A>C