Canonical Allele Identifier: PA2741858772
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2909245
ClinVar RCV Id: RCV003603814

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303619.1:p.Ala677Val
CA371307555
NM_001316690.1:c.2030C>T