Canonical Allele Identifier: PA2829068995
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1439710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373067.1:p.Pro7Thr
CA415172537
NM_001386138.1:c.19C>A