Canonical Allele Identifier: PA2829884813
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1418416
ClinVar RCV Id: RCV001930929
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060250.2:p.Ile2725Val
CA177329150
NM_017780.4:c.8173A>G