Canonical Allele Identifier: PA215908
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 41844
ClinVar RCV Id: RCV000034776 RCV000411681 RCV000410582 RCV000701145 RCV001023532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Thr170Ile
CA009269
NM_020630.6:c.509C>T