ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA645444193
Gene: CHRND
HGNC
NCBI
Linked Data
ClinVar Variation Id:
286380
ClinVar RCV Id:
RCV000360639
RCV000764382
RCV001855172
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000742.1:p.Arg407Gln
CA2168293
NM_000751.2:c.1220G>A