Canonical Allele Identifier: PA165957
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141618
ClinVar RCV Id: RCV000130211 RCV000409211 RCV000484737 RCV000765788 RCV001157265 RCV002222403 RCV003650393
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Met2213Ile
CA012330
NM_001127510.3:c.6639G>A
CA16035852
NM_001127510.3:c.6639G>C
CA16035853
NM_001127510.3:c.6639G>T