Canonical Allele Identifier: PA2827990170
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 946346
ClinVar RCV Id: RCV003650722
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Arg2629Thr
CA16038730
NM_001354900.2:c.7886G>C