Canonical Allele Identifier: PA163072
Gene: HNRNPA1 HGNC NCBI

Linked Data

ClinVar Variation Id: 135604
ClinVar RCV Id: RCV000122453

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002127.1:p.Phe296Leu
CA163071
NM_002136.4:c.886T>C
CA385122510
NM_002136.4:c.888T>G
CA385122511
NM_002136.4:c.888T>A