Canonical Allele Identifier: PA163058
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_112420.1:p.Asn332Ser
CA163056
NM_031157.4:c.995A>G