Canonical Allele Identifier: PA2825636926
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1022241
ClinVar RCV Id: RCV003770747
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Lys39Asn
CA360612028
NM_001127511.3:c.117G>C
CA360612030
NM_001127511.3:c.117G>T