Canonical Allele Identifier: PA645510059
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 438874
ClinVar RCV Id: RCV000507702
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Ser1038Phe
CA16028157
NM_001127510.3:c.3113C>T