Canonical Allele Identifier: PA2828022829
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 142246
ClinVar RCV Id: RCV000131255 RCV000148368 RCV000587871 RCV001175337 RCV003534386 RCV003998094
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341835.1:p.Arg1357Trp
CA009806
NM_001354906.2:c.4069C>T