Canonical Allele Identifier: PA2827964479
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2844378
ClinVar RCV Id: RCV003652473

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Ser359Arg
CA16023822
NM_001354898.2:c.1075A>C
CA16023828
NM_001354898.2:c.1077T>A
CA16023829
NM_001354898.2:c.1077T>G