Canonical Allele Identifier: PA161935
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 41839
ClinVar RCV Id: RCV000034768 RCV000121986 RCV000271726 RCV000311573 RCV000368621 RCV000393823 RCV000563975 RCV001080638 RCV002307371
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Arg67His
CA008548
NM_020630.6:c.200G>A