Canonical Allele Identifier: PA645450568
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 299891
ClinVar RCV Id: RCV000312196 RCV000313283 RCV000370252 RCV000393718 RCV000654549 RCV002321978 RCV003480586
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Val388Ile
CA031971
NM_020975.6:c.1162G>A