Canonical Allele Identifier: PA1139739202
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 844169
ClinVar RCV Id: RCV002339237 RCV003649309
ClinVar Variation Id: 1001543
ClinVar RCV Id: RCV001751567 RCV003166668 RCV003652128
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Thr1574Ser
CA16031563
NM_001354896.2:c.4720A>T
CA16031564
NM_001354896.2:c.4721C>G