Canonical Allele Identifier: PA658687488
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489456

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ile1557Asn
CA16031568
NM_001127510.3:c.4670T>A