Canonical Allele Identifier: PA1139741061
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 972422
ClinVar RCV Id: RCV001248449
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Leu94Val
CA376770477
NM_020975.6:c.280C>G