Canonical Allele Identifier: PA2827971932
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2677427
ClinVar RCV Id: RCV003471648
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser2649Phe
CA16038755
NM_001354898.2:c.7946C>T