Canonical Allele Identifier: PA2826952716
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_001302458.1:p.Asp2743Glu
CA207872
NM_001315529.2:c.8229C>A
CA410574812
NM_001315529.2:c.8229C>G