Canonical Allele Identifier: PA2825644669
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1760789
ClinVar RCV Id: RCV002412102
ClinVar Variation Id: 2106397
ClinVar RCV Id: RCV003308437 RCV003744913
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120983.2:p.Gly2592Arg
CA16038337
NM_001127511.3:c.7774G>A
CA16038338
NM_001127511.3:c.7774G>C