Canonical Allele Identifier: PA645451057
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 299898
ClinVar RCV Id: RCV000272691 RCV000307731 RCV000362457 RCV000393505 RCV001015632 RCV002520586
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Gly823Arg
CA10635707
NM_020975.6:c.2467G>A
CA376556286
NM_020975.6:c.2467G>C