Canonical Allele Identifier: PA2827970915
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 659672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001341827.1:p.Pro2344Leu
CA16036808
NM_001354898.2:c.7031C>T