Canonical Allele Identifier: PA2827968834
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 627841
ClinVar RCV Id: RCV000771706 RCV002536621 RCV003999959
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Met1707Leu
CA16032681
NM_001354898.2:c.5119A>C
CA16032682
NM_001354898.2:c.5119A>T