Canonical Allele Identifier: PA107011
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 13935
ClinVar RCV Id: RCV000014960 RCV000014961 RCV000021849 RCV000182583 RCV002453262
ClinVar Variation Id: 38612
ClinVar RCV Id: RCV000163610 RCV000339507 RCV000539138 RCV000709758 RCV000984325 RCV003466882 RCV003483444
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Leu790Phe
CA008702
NM_020975.6:c.2370G>C
CA008709
NM_020975.6:c.2370G>T