Canonical Allele Identifier: PA167137
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142015
ClinVar RCV Id: RCV000130799 RCV000484966 RCV002514736 RCV003650396 RCV003998080
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Leu1231Val
CA008636
NM_001127510.3:c.3691C>G