Canonical Allele Identifier: PA2741858773
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2880622
ClinVar RCV Id: RCV003602790
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303619.1:p.Ala677Ser
CA371307552
NM_001316690.1:c.2029G>T