ClinGen Allele Registry
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Canonical Allele Identifier:
PA916047995
Gene: PRSS56
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar RCV:
RCV000162043
ClinVar Variation:
183175
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001356777.1:p.Gly520Arg
CA186010
NM_001369848.1:c.1558G>A
CA2167806
NM_001369848.1:c.1558G>C