Canonical Allele Identifier: PA2827971041
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181817
ClinVar RCV Id: RCV000159569
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Asn2380Ser
CA012942
NM_001354898.2:c.7139A>G