Canonical Allele Identifier: PA658668222
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 486338
ClinVar RCV Id: RCV000562690 RCV002528996 RCV003459401
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Ser832Arg
CA039457
NM_020975.6:c.2496C>G
CA376556382
NM_020975.6:c.2494A>C
CA376556386
NM_020975.6:c.2496C>A