Canonical Allele Identifier: PA2825020780
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_000029.2:p.Thr1556Ser
CA16031563
NM_000038.6:c.4666A>T
CA16031564
NM_000038.6:c.4667C>G