Canonical Allele Identifier: PA2826143782
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_001171658.1:p.Val461Met
CA9878327
NM_001184729.3:c.1381G>A