Canonical Allele Identifier: PA2580357347
Gene: ANKRD11 HGNC NCBI

Linked Data

ClinVar Variation Id: 2442504
ClinVar RCV Id: RCV003149276
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_037407.4:p.Ser2110Cys
CA8241494
NM_013275.6:c.6329C>G