Canonical Allele Identifier: PA2828029229
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 489497
ClinVar RCV Id: RCV000579926
ClinVar Variation Id: 2452770
ClinVar RCV Id: RCV003177544
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Lys2331Asn
CA16038369
NM_001354906.2:c.6993A>C
CA16038370
NM_001354906.2:c.6993A>T