Canonical Allele Identifier: PA2573078743
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143738

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001373068.1:p.Pro79Leu
CA270574
NM_001386139.1:c.236C>T