Canonical Allele Identifier: PA916040534
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 411385

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Asn1734Ser
CA040767
NM_001354896.2:c.5201A>G