ClinGen Allele Registry
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Canonical Allele Identifier:
PA210742
Gene: F13B
HGNC
NCBI
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001985.2:p.Arg115His
CA210740
NM_001994.3:c.344G>A