Canonical Allele Identifier: PA106764
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13943
ClinVar RCV Id: RCV000014970 RCV000021802 RCV000489707 RCV001013426 RCV004018626
ClinVar Variation Id: 38602
ClinVar RCV Id: RCV000021798 RCV002408487
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Cys620Ser
CA008047
NM_020975.6:c.1858T>A
CA008085
NM_020975.6:c.1859G>C