Canonical Allele Identifier: PA2826635499
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 418325
ClinVar RCV Id: RCV000485501 RCV000629981 RCV000575218 RCV001192454
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Asp347Tyr
CA16617662
NM_001281494.2:c.1039G>T