Canonical Allele Identifier: PA2825015995
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_000029.2:p.Val642Leu
CA16025521
NM_000038.6:c.1924G>C
CA16025522
NM_000038.6:c.1924G>T