Canonical Allele Identifier: PA2825637635
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1368407
ClinVar RCV Id: RCV003772579

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser272Arg
CA16023216
NM_001127511.3:c.814A>C
CA16023221
NM_001127511.3:c.816T>A
CA16023222
NM_001127511.3:c.816T>G