Canonical Allele Identifier: PA891859121
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 572572
ClinVar RCV Id: RCV001525889 RCV003768062
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Asn627Ser
CA16025430
NM_001127510.3:c.1880A>G