Canonical Allele Identifier: PA2826625123
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 186227
ClinVar RCV Id: RCV000165781 RCV000168235 RCV000588989 RCV000758602 RCV003320582 RCV003468757
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Arg168Gln
CA016611
NM_001281492.2:c.503G>A