ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA645399310
Gene: PCNT
HGNC
NCBI
Linked Data
ClinVar Variation Id:
436202
ClinVar RCV Id:
RCV000502860
RCV001857142
RCV003424063
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Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_006022.3:p.Val1894Ile
CA10080059
NM_006031.5:c.5680G>A