Canonical Allele Identifier: PA1139676532
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 922523
ClinVar RCV Id: RCV001182640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ile1313Val
CA346761494
NM_000179.3:c.3937A>G