Canonical Allele Identifier: PA891859691
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 570865
ClinVar RCV Id: RCV001186456 RCV003534601 RCV003999569
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr2356Ala
CA046771
NM_001127510.3:c.7066A>G