Canonical Allele Identifier: PA2827974059
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 246087
ClinVar RCV Id: RCV000236999 RCV000491475 RCV000501897 RCV002519828 RCV003535657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Lys488Asn
CA10584241
NM_001354899.2:c.1464G>C
CA16024690
NM_001354899.2:c.1464G>T