Canonical Allele Identifier: PA2829070014
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143480

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373068.1:p.Glu260Asp
CA232945
NM_001386139.1:c.780G>C
CA415162879
NM_001386139.1:c.780G>T