Canonical Allele Identifier: PA2825644371
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 433676

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Pro2491Ser
CA16037691
NM_001127511.3:c.7471C>T