Canonical Allele Identifier: PA2827990581
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141436
ClinVar RCV Id: RCV000129949 RCV000198030 RCV000283075 RCV000515282 RCV000656753 RCV002267871 RCV003534376
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser2756Gly
CA015444
NM_001354900.2:c.8266A>G