Canonical Allele Identifier: PA1139673315
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 816914
ClinVar RCV Id: RCV001007927

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.Ser77Leu
CA415177555
NM_001110792.2:c.230C>T