Canonical Allele Identifier: PA2825638636
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_001120983.2:p.Val624Leu
CA16025521
NM_001127511.3:c.1870G>C
CA16025522
NM_001127511.3:c.1870G>T