Canonical Allele Identifier: PA916021790
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 529123
ClinVar RCV Id: RCV000634423

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303619.1:p.Pro727Ser
CA4760989
NM_001316690.1:c.2179C>T