Canonical Allele Identifier: PA2826951495
Gene: PCNT HGNC NCBI

Linked Data

ClinVar Variation Id: 1938739
ClinVar RCV Id: RCV002646499
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001302458.1:p.Gln870His
CA322005844
NM_001315529.2:c.2610G>T
CA410569719
NM_001315529.2:c.2610G>C