Canonical Allele Identifier: PA916011942
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 185611
ClinVar RCV Id: RCV000165060 RCV000201982 RCV000410385 RCV000656900 RCV001082754 RCV003323297
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Val858Ile
CA013029
NM_001281494.2:c.2572G>A