Canonical Allele Identifier: PA2827971581
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 573707

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser2544Arg
CA16038066
NM_001354898.2:c.7630A>C
CA16038072
NM_001354898.2:c.7632T>A
CA16038073
NM_001354898.2:c.7632T>G