Canonical Allele Identifier: PA2825544426
Gene: ERLIN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 226427
ClinVar RCV Id: RCV000211706

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001094096.1:p.Gly50Val
CA10576346
NM_001100626.2:c.149G>T