Canonical Allele Identifier: PA2826759688
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 328186
ClinVar RCV Id: RCV000291965 RCV003556342
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276033.1:p.Pro305Leu
CA9213063
NM_001289104.2:c.914C>T