Canonical Allele Identifier: PA151439
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 41523
ClinVar RCV Id: RCV000034408 RCV000115079 RCV000120013 RCV000168362 RCV000350760 RCV003492324 RCV003743549
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Asp1058Gly
CA008117
NM_000038.6:c.3173A>G