Canonical Allele Identifier: PA2827941415
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 231954

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341824.1:p.Ser634Arg
CA10578330
NM_001354895.2:c.1902T>G
CA16025473
NM_001354895.2:c.1900A>C
CA16025479
NM_001354895.2:c.1902T>A