Canonical Allele Identifier: PA2827962587
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489497
ClinVar RCV Id: RCV000579926
ClinVar Variation Id: 2452770
ClinVar RCV Id: RCV003177544

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Lys2624Asn
CA16038369
NM_001354897.2:c.7872A>C
CA16038370
NM_001354897.2:c.7872A>T