Canonical Allele Identifier: PA106977
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 372078
ClinVar RCV Id: RCV000410477 RCV000409178 RCV000704852 RCV002429338 RCV002505998 RCV004529566
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Gly830Arg
CA039416
NM_020975.6:c.2488G>A
CA376556360
NM_020975.6:c.2488G>C