Canonical Allele Identifier: PA2825020688
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2444634
ClinVar RCV Id: RCV003154402
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Gly1534Arg
CA16031406
NM_000038.6:c.4600G>A
CA16031407
NM_000038.6:c.4600G>C