Canonical Allele Identifier: PA645450961
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 372079
ClinVar RCV Id: RCV000409130 RCV000410654 RCV000565078 RCV000795272
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Val706Met
CA037364
NM_020975.6:c.2116G>A