Canonical Allele Identifier: PA916041539
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 482473

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Ser2580Gly
CA16038018
NM_001354896.2:c.7738A>G