Canonical Allele Identifier: PA2827962122
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 229765

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Pro2481Leu
CA10578443
NM_001354897.2:c.7442C>T