Canonical Allele Identifier: PA144799
Gene: HNRNPA2B1 HGNC NCBI

Linked Data

ClinVar Variation Id: 65454
ClinVar RCV Id: RCV000055652
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002128.1:p.Asp290Val
CA144798
NM_002137.4:c.869A>T