Canonical Allele Identifier: PA2827959419
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2655637
ClinVar RCV Id: RCV003429729
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Thr1657Lys
CA16032149
NM_001354897.2:c.4970C>A