Canonical Allele Identifier: PA645450394
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 299886
ClinVar RCV Id: RCV000270926 RCV000323687 RCV000329067 RCV000363157 RCV000551141 RCV001014798 RCV003153553
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Gly74Ser
CA037807
NM_020975.6:c.220G>A