Canonical Allele Identifier: PA2829069256
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 429415

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373067.1:p.Pro139Ser
CA415168068
NM_001386138.1:c.415C>T