Canonical Allele Identifier: PA2827989833
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 573707
ClinVar RCV Id: RCV001026737 RCV003999638 RCV003534640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341829.1:p.Ser2528Arg
CA16038066
NM_001354900.2:c.7582A>C
CA16038072
NM_001354900.2:c.7584T>A
CA16038073
NM_001354900.2:c.7584T>G