Canonical Allele Identifier: PA2827962223
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1759217
ClinVar Variation Id: 1759218
ClinVar RCV Id: RCV002391624

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Gln2510His
CA16037641
NM_001354897.2:c.7530G>C
CA16037642
NM_001354897.2:c.7530G>T