Canonical Allele Identifier: PA2825626788
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2822243
ClinVar RCV Id: RCV003650976
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Cys447Ser
CA16024236
NM_001127510.3:c.1339T>A
CA16024240
NM_001127510.3:c.1340G>C