Canonical Allele Identifier: PA2826956228
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 138195

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Pro309Leu
CA199300
NM_001316337.2:c.926C>T