Canonical Allele Identifier: PA2826593702
Gene: ANXA11 HGNC NCBI

Linked Data

ClinVar Variation Id: 488354

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265336.1:p.Gly38Arg
CA5576379
NM_001278407.2:c.112G>A
CA377368837
NM_001278407.2:c.112G>C