Canonical Allele Identifier: PA2827974426
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2830039
ClinVar RCV Id: RCV003744312
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341828.1:p.Val614Leu
CA16025521
NM_001354899.2:c.1840G>C
CA16025522
NM_001354899.2:c.1840G>T