Canonical Allele Identifier: PA2829068396
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143652

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373066.1:p.Pro2Thr
CA232991
NM_001386137.1:c.4C>A