Canonical Allele Identifier: PA645398552
Gene: PCNT HGNC NCBI

Linked Data

ClinVar Variation Id: 436247
ClinVar RCV Id: RCV000501156
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006022.3:p.Thr1013Ile
CA10079154
NM_006031.5:c.3038C>T