Canonical Allele Identifier: PA658670277
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 486321
ClinVar RCV Id: RCV000575489 RCV000709102 RCV000812605 RCV003459399 RCV001764690 RCV002483540
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Asn151Ser
CA043742
NM_020975.6:c.452A>G