Canonical Allele Identifier: PA156772
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 127288
ClinVar RCV Id: RCV000120024 RCV000411300 RCV000565031 RCV000985246 RCV000677784 RCV001154639 RCV003534336
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000029.2:p.Ser1126Arg
CA008342
NM_000038.6:c.3378C>G
CA16028729
NM_000038.6:c.3376A>C
CA16028734
NM_000038.6:c.3378C>A