Canonical Allele Identifier: PA916043064
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 24881
ClinVar RCV Id: RCV000148776 RCV000231209 RCV000567555 RCV000679758 RCV000709104 RCV001818171 RCV003460487 RCV004528128
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Gly67Arg
CA009403
NM_001355216.1:c.199G>A
CA376546111
NM_001355216.1:c.199G>C