Canonical Allele Identifier: PA272965
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 161360
ClinVar RCV Id: RCV000148786 RCV000197537 RCV000410075 RCV000412078 RCV001024031 RCV001294034 RCV003736605
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Arg180Gln
CA009280
NM_020975.6:c.539G>A