Canonical Allele Identifier: PA2826630037
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 428381
ClinVar RCV Id: RCV000491842 RCV001851340
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Gly128Glu
CA346744168
NM_001281493.2:c.383G>A