Canonical Allele Identifier: PA128227
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 24908
ClinVar RCV Id: RCV000418588 RCV000429498 RCV000436253 RCV000654593 RCV000428845 RCV000440788
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Cys630Arg
CA008145
NM_020975.6:c.1888T>C