Canonical Allele Identifier: PA2828000592
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3222005
ClinVar RCV Id: RCV004513423

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Asn511Thr
CA16025269
NM_001354902.2:c.1532A>C