Canonical Allele Identifier: PA915992832
Gene: PGM1 HGNC NCBI

Linked Data

ClinVar Variation Id: 39771
ClinVar RCV Id: RCV000032990
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001166289.1:p.Gly139Arg
CA130545
NM_001172818.1:c.415G>C
CA340646148
NM_001172818.1:c.415G>A