Canonical Allele Identifier: PA2827971750
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2765432
ClinVar RCV Id: RCV003538114

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Pro2597Ser
CA16038421
NM_001354898.2:c.7789C>T