Canonical Allele Identifier: PA2826629742
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 419950
ClinVar RCV Id: RCV000563224 RCV000629709 RCV001704606 RCV004003316
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268422.1:p.Ser58Gly
CA067126
NM_001281493.2:c.172A>G