Canonical Allele Identifier: PA215901
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 41842
ClinVar RCV Id: RCV000034773 RCV000123312 RCV000409480 RCV000410572 RCV000562304 RCV000763649 RCV002477060 RCV003387739
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Val871Ile
CA008940
NM_020975.6:c.2611G>A