Canonical Allele Identifier: PA215897
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 41841
ClinVar RCV Id: RCV000034772 RCV000663125 RCV000698313 RCV001015867
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Met848Lys
CA008905
NM_020975.6:c.2543T>A