Canonical Allele Identifier: PA2827965259
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127279
ClinVar RCV Id: RCV000115071
ClinVar Variation Id: 628655
ClinVar RCV Id: RCV000773312 RCV003322819 RCV003744640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ile613Leu
CA006331
NM_001354898.2:c.1837A>T
CA16025497
NM_001354898.2:c.1837A>C