Canonical Allele Identifier: PA2826628815
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 920280
ClinVar RCV Id: RCV001178948 RCV001361175
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Leu1105Phe
CA346760985
NM_001281492.2:c.3313C>T