Canonical Allele Identifier: PA658670299
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 477378
ClinVar RCV Id: RCV000526271 RCV001105728 RCV001105729 RCV001105730 RCV001105731 RCV002350393
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Arg189His
CA043969
NM_020975.6:c.566G>A