ClinGen Allele Registry
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Canonical Allele Identifier:
PA2826942200
Gene: CHRND
HGNC
NCBI
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001298124.1:p.Ala61Pro
CA350998301
NM_001311195.2:c.181G>C