Canonical Allele Identifier: PA156881
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133537
ClinVar RCV Id: RCV000120047 RCV000163521 RCV000199434 RCV000677785 RCV000677786 RCV000677787 RCV001704030 RCV003952585
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ala2760Ser
CA014561
NM_001127511.3:c.8278G>T