Canonical Allele Identifier: PA198347
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 187701
ClinVar RCV Id: RCV000167451 RCV000409934 RCV000409277 RCV000654567 RCV000764899
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Thr742Met
CA008602
NM_020630.6:c.2225C>T