Canonical Allele Identifier: PA658805622
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 543760
ClinVar RCV Id: RCV000654601 RCV000663067 RCV001019124 RCV002284419 RCV002507130
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Pro1067Ser
CA054755
NM_020975.6:c.3199C>T