Canonical Allele Identifier: PA2827986053
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 135701

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ile1376Leu
CA009397
NM_001354900.2:c.4126A>C