Canonical Allele Identifier: PA2827993860
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 822912
ClinVar RCV Id: RCV001018680
ClinVar Variation Id: 2452689
ClinVar RCV Id: RCV003177463

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Asn978Lys
CA16028150
NM_001354901.2:c.2934C>A
CA16028151
NM_001354901.2:c.2934C>G