Canonical Allele Identifier: PA916010409
Gene: ANXA11 HGNC NCBI

Linked Data

ClinVar Variation Id: 488353
ClinVar RCV Id: RCV000578138 RCV001853834 RCV003403366
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265338.1:p.Asp7Gly
CA377368826
NM_001278409.2:c.20A>G