Canonical Allele Identifier: PA2827971900
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 565362
ClinVar RCV Id: RCV004026176 RCV003534550
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Pro2640Ser
CA16038695
NM_001354898.2:c.7918C>T