Canonical Allele Identifier: PA2826759251
Gene: PRKCSH HGNC NCBI

Linked Data

ClinVar Variation Id: 328180

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001276031.1:p.Ala251Val
CA9212963
NM_001289102.2:c.752C>T