ClinGen Allele Registry
Allele Registry
Register
Login
Forgot Login?
Canonical Allele Identifier:
PA110470
Gene: CHRND
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000020034
ClinVar Variation:
18366
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000742.1:p.Glu80Lys
CA128066
NM_000751.2:c.238G>A