Canonical Allele Identifier: PA2828012467
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2861029
ClinVar RCV Id: RCV003743178
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341831.1:p.Trp2521Ser
CA16038351
NM_001354902.2:c.7562G>C