Canonical Allele Identifier: PA2828325048
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143547

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Val29Ala
CA170290
NM_001369391.2:c.86T>C