Canonical Allele Identifier: PA161958
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 24880
ClinVar RCV Id: RCV000034779 RCV000121992 RCV000276548 RCV000333869 RCV000354891 RCV000367517 RCV000565970 RCV000755685 RCV001083006 RCV003492298
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Val292Met
CA009374
NM_020975.6:c.874G>A