Canonical Allele Identifier: PA916041493
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 156483

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Tyr2535Cys
CA013809
NM_001354896.2:c.7604A>G