Canonical Allele Identifier: PA2826634887
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 233297
ClinVar RCV Id: RCV000218406 RCV000466630 RCV000481397 RCV003469072 RCV003998046
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Val207Leu
CA10578073
NM_001281494.2:c.619G>C
CA346746442
NM_001281494.2:c.619G>T