Canonical Allele Identifier: PA2828013421
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 3069608
ClinVar RCV Id: RCV004008152 RCV004371939
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341834.1:p.Arg2513Ser
CA16038748
NM_001354905.2:c.7539A>C
CA16038749
NM_001354905.2:c.7539A>T