Canonical Allele Identifier: PA2827959134
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489456

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ile1567Asn
CA16031568
NM_001354897.2:c.4700T>A