Canonical Allele Identifier: PA916041589
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_001341825.1:p.Lys2632Asn
CA16038369
NM_001354896.2:c.7896A>C
CA16038370
NM_001354896.2:c.7896A>T