Canonical Allele Identifier: PA645450597
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 299892
ClinVar RCV Id: RCV000292520 RCV000352045 RCV000402202 RCV000390089 RCV003469251 RCV001840481 RCV001239526 RCV002392835 RCV004529483
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Arg474Trp
CA033490
NM_020975.6:c.1420C>T