Canonical Allele Identifier: PA891847838
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 566200
ClinVar RCV Id: RCV000685948
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Ser110Asn
CA043134
NM_020975.6:c.329G>A