Canonical Allele Identifier: PA2826952674
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_001302458.1:p.Gln2674Arg
CA173121
NM_001315529.2:c.8021A>G