Canonical Allele Identifier: PA2827978661
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411367
ClinVar RCV Id: RCV000457967 RCV000561037 RCV000679070 RCV004001924
ClinVar Variation Id: 630647
ClinVar RCV Id: RCV000776593 RCV003744648
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Thr1904Ser
CA043023
NM_001354899.2:c.5710A>T
CA16034011
NM_001354899.2:c.5711C>G