Canonical Allele Identifier: PA333788
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 183069
ClinVar RCV Id: RCV000161934 RCV000236412 RCV000568367 RCV003998534 RCV003315967 RCV003398826
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asp1636Tyr
CA009798
NM_000038.6:c.4906G>T