Canonical Allele Identifier: PA128321
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 24931
ClinVar RCV Id: RCV000021838 RCV000148771 RCV000567780 RCV001582493 RCV002496436 RCV002466411 RCV004018657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Lys666Glu
CA008502
NM_020630.6:c.1996A>G