Canonical Allele Identifier: PA2828033951
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231954

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Ser508Arg
CA10578330
NM_001354904.2:c.1524T>G
CA16025473
NM_001354904.2:c.1522A>C
CA16025479
NM_001354904.2:c.1524T>A