Canonical Allele Identifier: PA164921
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 141253
ClinVar RCV Id: RCV000129685 RCV003743585
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Tyr1027His
CA008031
NM_001127510.3:c.3079T>C