Canonical Allele Identifier: PA645378201
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 410435
ClinVar RCV Id: RCV000765675 RCV000461408 RCV000573037 RCV000480657 RCV001192488 RCV003463931
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala35Val
CA067076
NM_000179.3:c.104C>T