Canonical Allele Identifier: PA2573078696
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143652

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373068.1:p.Pro2Thr
CA232991
NM_001386139.1:c.4C>A