Canonical Allele Identifier: PA2828012321
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 573707

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Ser2478Arg
CA16038066
NM_001354902.2:c.7432A>C
CA16038072
NM_001354902.2:c.7434T>A
CA16038073
NM_001354902.2:c.7434T>G