Canonical Allele Identifier: PA2827973371
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 822781
ClinVar RCV Id: RCV001018420

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser267Arg
CA16023248
NM_001354899.2:c.799A>C
CA16023252
NM_001354899.2:c.801T>A
CA16023253
NM_001354899.2:c.801T>G