Canonical Allele Identifier: PA2829939614
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 568416
ClinVar RCV Id: RCV000688770 RCV001103793 RCV001103794 RCV001103791 RCV001103792
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Pro162Ser
CA376543214
NM_020630.6:c.484C>T