Canonical Allele Identifier: PA2826627891
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 237168
ClinVar RCV Id: RCV000231932 RCV000571874 RCV000581651 RCV001589169 RCV003463639 RCV003998722 RCV004529388
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ile814Val
CA10582071
NM_001281492.2:c.2440A>G