Canonical Allele Identifier: PA2825644334
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 487060
ClinVar RCV Id: RCV000565939 RCV003744577
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Ser2479Trp
CA16037624
NM_001127511.3:c.7436C>G