Canonical Allele Identifier: PA170262
Gene: MECP2 HGNC NCBI

Linked Data

ClinVar Variation Id: 143493
ClinVar RCV Id: RCV000133024 RCV003483516 RCV001857482
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001104262.1:p.His63Gln
CA170260
NM_001110792.2:c.189C>G
CA415177857
NM_001110792.2:c.189C>A