Canonical Allele Identifier: PA2829069790
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 36490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373068.1:p.Pro161Leu
CA199482
NM_001386139.1:c.482C>T