Canonical Allele Identifier: PA2580319397
Gene: PCNT HGNC NCBI

Linked Data

ClinVar Variation Id: 1938739
ClinVar RCV Id: RCV002646499
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006022.3:p.Gln988His
CA322005844
NM_006031.5:c.2964G>T
CA410569719
NM_006031.5:c.2964G>C