Canonical Allele Identifier: PA2826594080
Gene: ANXA11 HGNC NCBI

Linked Data

ClinVar Variation Id: 488354
ClinVar RCV Id: RCV000578149 RCV003105971 RCV001860003 RCV003962641
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265337.1:p.Gly38Arg
CA5576379
NM_001278408.2:c.112G>A
CA377368837
NM_001278408.2:c.112G>C