Canonical Allele Identifier: PA645451180
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 241356
ClinVar RCV Id: RCV000228519 RCV000567853 RCV001589196 RCV001820760 RCV002500812
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Thr1038Ile
CA042623
NM_020975.6:c.3113C>T