Canonical Allele Identifier: PA163036
Gene: HNRNPA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 135592
ClinVar RCV Id: RCV000122441
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002127.1:p.Phe263Leu
CA163035
NM_002136.4:c.787T>C
CA6606394
NM_002136.4:c.789T>G
CA385122298
NM_002136.4:c.789T>A