Canonical Allele Identifier: PA337179
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 216727
ClinVar RCV Id: RCV000197380 RCV000571944 RCV000678743 RCV000679750 RCV000662413 RCV002503785 RCV003153474 RCV003462339
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Glu136Lys
CA043648
NM_020630.6:c.406G>A