Canonical Allele Identifier: PA2827956106
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231954

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Ser644Arg
CA10578330
NM_001354897.2:c.1932T>G
CA16025473
NM_001354897.2:c.1930A>C
CA16025479
NM_001354897.2:c.1932T>A