Canonical Allele Identifier: PA121714
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 11841

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Pro237Leu
CA121713
NM_001110792.2:c.710C>T