Canonical Allele Identifier: PA297805
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 181799
ClinVar RCV Id: RCV000159547 RCV000211907 RCV000234536 RCV003315947 RCV002307414
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Thr1082Ser
CA008176
NM_001127510.3:c.3245C>G
CA16028451
NM_001127510.3:c.3244A>T