Canonical Allele Identifier: PA2827953181
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2815299
ClinVar RCV Id: RCV003744126
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Arg2488Ser
CA16037460
NM_001354896.2:c.7464A>C
CA16037461
NM_001354896.2:c.7464A>T