Allele Registry

Canonical Allele Identifier: PA163042

Gene: HNRNPA1 HGNC NCBI

ClinVar Allele:

139320

ClinVar RCV:

RCV000122443

ClinVar Variation:

135594

HGVS (amino-acid)	Matching Registered Transcripts
NP_002127.1:p.Phe273Leu	CA163041 NM_002136.4:c.817T>C CA385122363 NM_002136.4:c.819T>A CA385122364 NM_002136.4:c.819T>G