ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA1139680209
Gene: CHRND
HGNC
NCBI
Linked Data
ClinVar Variation Id:
835938
ClinVar RCV Id:
RCV001036943
RCV004031012
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000742.1:p.Asp440Val
CA2168322
NM_000751.2:c.1319A>T