Canonical Allele Identifier: PA2827945071
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 486737

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Gln1749His
CA16032805
NM_001354895.2:c.5247G>C
CA16032806
NM_001354895.2:c.5247G>T