Canonical Allele Identifier: PA297743
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181787
ClinVar RCV Id: RCV000159532 RCV000230899 RCV000656745 RCV000579996 RCV003534399 RCV003998404
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Met413Val
CA004131
NM_001127511.3:c.1237A>G