Canonical Allele Identifier: PA645485999
Gene: CRADD HGNC NCBI

Linked Data

ClinVar Variation Id: 372191
ClinVar RCV Id: RCV000412611 RCV001261380
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003796.1:p.Arg170His
CA6720248
NM_003805.5:c.509G>A