Canonical Allele Identifier: PA2828033898
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1714967
ClinVar RCV Id: RCV003743845
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341833.1:p.Thr502Ser
CA16025436
NM_001354904.2:c.1504A>T
CA16025438
NM_001354904.2:c.1505C>G