Canonical Allele Identifier: PA2827989938
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1343462
ClinVar RCV Id: RCV001844480 RCV002406906
ClinVar Variation Id: 1378873
ClinVar RCV Id: RCV003745382
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser2560Arg
CA16038274
NM_001354900.2:c.7678A>C
CA16038280
NM_001354900.2:c.7680T>A
CA16038281
NM_001354900.2:c.7680T>G