Canonical Allele Identifier: PA2828047423
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490359
ClinVar RCV Id: RCV000581826 RCV001174584 RCV002232546
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Val2310Leu
CA16037242
NM_001354904.2:c.6928G>C
CA16037243
NM_001354904.2:c.6928G>T