Canonical Allele Identifier: PA2826143959
Gene: PIGT HGNC NCBI

Linked Data

ClinVar Variation Id: 440973
ClinVar RCV Id: RCV000509376 RCV000657935 RCV000990305
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171659.1:p.Val426Met
CA9878327
NM_001184730.3:c.1276G>A