Canonical Allele Identifier: PA163048
Gene: HNRNPA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 135596
ClinVar RCV Id: RCV000122445
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002127.1:p.Pro275Ser
CA163047
NM_002136.4:c.823C>T