Canonical Allele Identifier: PA207873
Gene: PCNT HGNC NCBI

Linked Data

ClinVar Variation Id: 211887
ClinVar RCV Id: RCV000194006
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006022.3:p.Asp2940Glu
CA207872
NM_006031.5:c.8820C>A
CA410574812
NM_006031.5:c.8820C>G