Canonical Allele Identifier: PA2826637221
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 135839
ClinVar RCV Id: RCV000132157 RCV000408980 RCV001030498 RCV001257068 RCV001355067 RCV003492535 RCV000588824 RCV004528840 RCV001796965
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Val749Ile
CA011639
NM_001281494.2:c.2245G>A