Canonical Allele Identifier: PA189983
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184763
ClinVar RCV Id: RCV000164075 RCV000226636 RCV000483633 RCV001582644 RCV003534437 RCV003937504 RCV003995310
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Arg2507His
CA013862
NM_001127511.3:c.7520G>A