Canonical Allele Identifier: PA2827962623
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760974

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asn2634Lys
CA16038436
NM_001354897.2:c.7902T>A
CA16038437
NM_001354897.2:c.7902T>G