Canonical Allele Identifier: PA2828325363
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001356320.1:p.Ala186Val
CA270535
NM_001369391.2:c.557C>T