Canonical Allele Identifier: PA2827957709
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 629986
ClinVar RCV Id: RCV000774851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Asp1144Gly
CA16028788
NM_001354897.2:c.3431A>G