Canonical Allele Identifier: PA2825638621
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2681902
ClinVar RCV Id: RCV003477194
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Gly617Arg
CA16025480
NM_001127511.3:c.1849G>A
CA16025481
NM_001127511.3:c.1849G>C