Canonical Allele Identifier: PA3057503539
Gene: CHD7 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Glu22Gly
CA371295348
NM_017780.4:c.65A>G