Canonical Allele Identifier: PA645450604
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 241336
ClinVar RCV Id: RCV000234316 RCV001011698 RCV001107800 RCV001107138 RCV000709111 RCV001107139 RCV001770206 RCV001107140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Thr488Ser
CA033750
NM_020975.6:c.1462A>T
CA376549755
NM_020975.6:c.1463C>G