Canonical Allele Identifier: PA2825636931
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 999340
ClinVar RCV Id: RCV003770490
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser40Arg
CA360612032
NM_001127511.3:c.118A>C
CA360612043
NM_001127511.3:c.120C>G
CA360612045
NM_001127511.3:c.120C>A