Canonical Allele Identifier: PA2826635793
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 142897
ClinVar RCV Id: RCV000132365 RCV000212659 RCV000411918 RCV000468830 RCV003998145
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Thr414Ile
CA009755
NM_001281494.2:c.1241C>T