Canonical Allele Identifier: PA2741888604
Gene: FTH1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2636131
ClinVar RCV Id: RCV003402863

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_002023.2:p.Asp172Asn
CA6041205
NM_002032.3:c.514G>A