Canonical Allele Identifier: PA2826636153
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89279
ClinVar RCV Id: RCV000074744 RCV000115389 RCV000212665 RCV000148650 RCV000409574 RCV000656572 RCV000524141 RCV000680176 RCV001353412 RCV001798252
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Val498Leu
CA010185
NM_001281494.2:c.1492G>C