Canonical Allele Identifier: PA106713
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13914
ClinVar RCV Id: RCV000014934 RCV000014933 RCV000082050 RCV000161938 RCV001013348
ClinVar Variation Id: 38601
ClinVar RCV Id: RCV000032040 RCV000182594 RCV000569893 RCV003233028 RCV004532475
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Cys618Ser
CA007974
NM_020975.6:c.1852T>A
CA008013
NM_020975.6:c.1853G>C