Canonical Allele Identifier: PA645398805
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 372035
ClinVar RCV Id: RCV000410953 RCV000677755 RCV001178393 RCV002230744
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Leu292Phe
CA051023
NM_001127510.3:c.876G>T
CA16023233
NM_001127510.3:c.876G>C