Canonical Allele Identifier: PA2827977403
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1742057
ClinVar RCV Id: RCV002342576
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Ser1517Pro
CA16031483
NM_001354899.2:c.4549T>C