Canonical Allele Identifier: PA2573180162
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1468919

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Val224Asp
CA415172922
NM_001110792.2:c.671T>A