Canonical Allele Identifier: PA156806
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 133522

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser2479Leu
CA013717
NM_001127511.3:c.7436C>T