Canonical Allele Identifier: PA891851544
Gene: PAM16 HGNC NCBI

Linked Data

ClinVar Variation Id: 585054
ClinVar RCV Id: RCV000709807 RCV002532893
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_057153.8:p.Arg38Gly
CA394603500
NM_016069.11:c.112C>G