Canonical Allele Identifier: PA2826143668
Gene: PIGT HGNC NCBI

Linked Data

ClinVar Variation Id: 252704
ClinVar RCV Id: RCV000239263 RCV000442187 RCV000990304
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001171658.1:p.Val123Leu
CA9877867
NM_001184729.3:c.367G>T
CA409166529
NM_001184729.3:c.367G>C