Canonical Allele Identifier: PA2826952092
Gene: PCNT HGNC NCBI

Linked Data

ClinVar Variation Id: 1407698
ClinVar RCV Id: RCV001937859

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001302458.1:p.Arg1813Cys
CA10080090
NM_001315529.2:c.5437C>T