Canonical Allele Identifier: PA2573078723
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143710

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373068.1:p.Ala56Val
CA270535
NM_001386139.1:c.167C>T