Canonical Allele Identifier: PA2828054008
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 939904

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.His492Gln
CA16025592
NM_001354905.2:c.1476C>A
CA16025593
NM_001354905.2:c.1476C>G