Canonical Allele Identifier: PA170261
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_004983.1:p.His51Gln
CA170260
NM_004992.4:c.153C>G
CA415177857
NM_004992.4:c.153C>A