Canonical Allele Identifier: PA2827966659
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_001341827.1:p.Thr1057Ser
CA008176
NM_001354898.2:c.3170C>G
CA16028451
NM_001354898.2:c.3169A>T