Canonical Allele Identifier: PA2828047502
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 2166006
ClinVar RCV Id: RCV003090274 RCV003294495
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Phe358Leu
CA376552771
NM_001355216.1:c.1072T>C
CA376552776
NM_001355216.1:c.1074C>A
CA376552777
NM_001355216.1:c.1074C>G