Canonical Allele Identifier: PA2829069331
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 36490

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373067.1:p.Pro161Leu
CA199482
NM_001386138.1:c.482C>T