Canonical Allele Identifier: PA163057
Gene: HNRNPA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 135599
ClinVar RCV Id: RCV000122448
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002127.1:p.Asn280Ser
CA163056
NM_002136.4:c.839A>G