Canonical Allele Identifier: PA2573078728
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143716

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373068.1:p.Ala64Pro
CA270538
NM_001386139.1:c.190G>C