Canonical Allele Identifier: PA106684
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13929
ClinVar RCV Id: RCV000014954 RCV000021792 RCV000114391 RCV000427260 RCV000345209 RCV000444839 RCV000434685 RCV000442341 RCV002256000
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Cys618Arg
CA007985
NM_020975.6:c.1852T>C