Canonical Allele Identifier: PA161932
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 36723
ClinVar RCV Id: RCV000034766 RCV000030402 RCV000121985 RCV000202649 RCV000163266 RCV000148768 RCV001082759 RCV001108849 RCV001108851 RCV001108850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Leu56Met
CA007702
NM_020975.6:c.166C>A