Canonical Allele Identifier: PA2828048506
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 220266
ClinVar RCV Id: RCV000205988 RCV001015870
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001342145.1:p.Met594Ile
CA039702
NM_001355216.1:c.1782G>A
CA376556524
NM_001355216.1:c.1782G>C
CA376556525
NM_001355216.1:c.1782G>T