ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA2828548409
Gene: FECH
HGNC
NCBI
Linked Data
ClinVar Variation Id:
1360747
ClinVar RCV Id:
RCV001907162
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001361707.1:p.Ile103Leu
CA402536813
NM_001374778.1:c.307A>C