Canonical Allele Identifier: PA2825644503
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 470102

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser2537Leu
CA16037984
NM_001127511.3:c.7610C>T