Canonical Allele Identifier: PA332947
Gene: RET HGNC NCBI

Linked Data

ClinVar Variation Id: 136120
ClinVar RCV Id: RCV000123322 RCV000411433 RCV000409019 RCV000563716 RCV001310569
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_066124.1:p.Arg112His
CA009221
NM_020975.6:c.335G>A