Canonical Allele Identifier: PA2827956004
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3222005
ClinVar RCV Id: RCV004513423

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asn612Thr
CA16025269
NM_001354897.2:c.1835A>C