Canonical Allele Identifier: PA167232
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142044
ClinVar RCV Id: RCV000130848 RCV000236813 RCV000409644 RCV001174857 RCV003905234 RCV003315899 RCV003492605
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Met2213Val
CA012319
NM_000038.6:c.6637A>G