Canonical Allele Identifier: PA2828455690
Gene: FECH HGNC NCBI
ClinVar RCV:
RCV000000584
ClinVar Variation:
554
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001358024.1:p.Val290Gly
CA251512
NM_001371095.1:c.869T>G