Canonical Allele Identifier: PA2827954388
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1362509
ClinVar RCV Id: RCV003772534
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Trp54Arg
CA360612206
NM_001354897.2:c.160T>A
CA360612207
NM_001354897.2:c.160T>C