Canonical Allele Identifier: PA2825644641
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1039177

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Thr2580Ser
CA16038256
NM_001127511.3:c.7738A>T
CA16038257
NM_001127511.3:c.7739C>G