Canonical Allele Identifier: PA2827971934
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 584680
ClinVar RCV Id: RCV000708975
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Pro2650Ser
CA16038758
NM_001354898.2:c.7948C>T