Canonical Allele Identifier: PA658667862
Gene: ERLIN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 424656

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_009106.1:p.Asp300Val
CA4711041
NM_007175.8:c.899A>T