Canonical Allele Identifier: PA2827991223
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 1062957
ClinVar RCV Id: RCV003771195
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341830.1:p.Met141Leu
CA16022641
NM_001354901.2:c.421A>C
CA16022643
NM_001354901.2:c.421A>T