Canonical Allele Identifier: PA2828046481
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 224354
ClinVar RCV Id: RCV000416603 RCV000560396 RCV001010283 RCV003468970
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Ser147Cys
CA032120
NM_001355216.1:c.439A>T