Canonical Allele Identifier: PA173122
Gene: PCNT HGNC NCBI

Linked Data

ClinVar Variation Id: 159671
ClinVar RCV Id: RCV000147222 RCV000608247 RCV001535234 RCV003975161
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006022.3:p.Gln2792Arg
CA173121
NM_006031.5:c.8375A>G