Canonical Allele Identifier: PA2827957348
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2624856

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Tyr1041Cys
CA16028105
NM_001354897.2:c.3122A>G