Canonical Allele Identifier: PA2825638659
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 939904

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.His634Gln
CA16025592
NM_001127511.3:c.1902C>A
CA16025593
NM_001127511.3:c.1902C>G