Canonical Allele Identifier: PA2827962551
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 490364

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser2611Asn
CA16038277
NM_001354897.2:c.7832G>A