Canonical Allele Identifier: PA128363
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 37102
ClinVar RCV Id: RCV000148773 RCV000182584 RCV000210181 RCV000499191 RCV000515232 RCV000586783 RCV001804750 RCV003153308 RCV003460494 RCV004528141
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_065681.1:p.Val804Met
CA008751
NM_020630.6:c.2410G>A