Canonical Allele Identifier: PA916043100
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 543741
ClinVar RCV Id: RCV000654577 RCV000709125 RCV001018329 RCV001106020 RCV001106021 RCV001106022 RCV001106023 RCV003318621 RCV003493698
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Leu764Phe
CA042397
NM_001355216.1:c.2290C>T