ClinGen Allele Registry
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Canonical Allele Identifier:
PA2825312571
Gene: FECH
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
331897
ClinVar RCV:
RCV000285620
RCV001521397
ClinVar Variation:
327434
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001012533.1:p.Arg102Gln
CA8973261
NM_001012515.4:c.305G>A