Canonical Allele Identifier: PA2827989964
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760789
ClinVar RCV Id: RCV002412102
ClinVar Variation Id: 2106397
ClinVar RCV Id: RCV003308437 RCV003744913
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Gly2569Arg
CA16038337
NM_001354900.2:c.7705G>A
CA16038338
NM_001354900.2:c.7705G>C