Canonical Allele Identifier: PA658660663
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482396
ClinVar RCV Id: RCV000569767 RCV003537148
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Met2491Ile
CA16037587
NM_001127510.3:c.7473G>A
CA16037588
NM_001127510.3:c.7473G>C
CA16037589
NM_001127510.3:c.7473G>T