Canonical Allele Identifier: PA2826956216
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 211454

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303266.1:p.Pro306Ser
CA206184
NM_001316337.2:c.916C>T