Canonical Allele Identifier: PA187892
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 184130
ClinVar RCV Id: RCV000163274 RCV000232978 RCV000236184 RCV000656748 RCV001353588 RCV003315992
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Leu2039Phe
CA010933
NM_001127510.3:c.6117G>T
CA16034721
NM_001127510.3:c.6117G>C