Canonical Allele Identifier: PA2741858770
Gene: CHD7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2812048
ClinVar RCV Id: RCV003604205
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001303619.1:p.Arg667Gly
CA371307368
NM_001316690.1:c.1999A>G