Canonical Allele Identifier: PA2573274708
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 1471458
ClinVar RCV Id: RCV001966786
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Val882Ile
CA376557131
NM_020975.6:c.2644G>A