Canonical Allele Identifier: PA916041587
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 537451
ClinVar RCV Id: RCV003538442
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341825.1:p.Trp2630Cys
CA16038354
NM_001354896.2:c.7890G>C
CA16038355
NM_001354896.2:c.7890G>T