Canonical Allele Identifier: PA658670195
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 486316
ClinVar RCV Id: RCV000575741 RCV000689589 RCV001821691 RCV004530620
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Leu11Met
CA206710333
NM_020975.6:c.31C>A