Canonical Allele Identifier: PA645398791
Gene: APC HGNC NCBI

Linked Data

ClinVar Variation Id: 419482

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001120982.1:p.Met271Ile
CA16023107
NM_001127510.3:c.813G>A
CA16023108
NM_001127510.3:c.813G>C
CA16023109
NM_001127510.3:c.813G>T