Canonical Allele Identifier: PA2742001641
Gene: ANKRD13A HGNC NCBI

Linked Data

ClinVar Variation Id: 2547720
ClinVar RCV Id: RCV004315459
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_149112.1:p.Val90Ala
CA386658134
NM_033121.2:c.269T>C