Canonical Allele Identifier: PA2827963047
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 2107310
ClinVar RCV Id: RCV003744920
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341826.1:p.Val2758Leu
CA16039217
NM_001354897.2:c.8272G>C
CA16039218
NM_001354897.2:c.8272G>T