Canonical Allele Identifier: PA2826635280
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 568709
ClinVar RCV Id: RCV000689151 RCV002397384
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Gly297Ala
CA346749323
NM_001281494.2:c.890G>C