Canonical Allele Identifier: PA2828048580
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 1002688
ClinVar RCV Id: RCV001299149
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Met614Ile
CA376556841
NM_001355216.1:c.1842G>A
CA376556842
NM_001355216.1:c.1842G>C
CA376556844
NM_001355216.1:c.1842G>T