Canonical Allele Identifier: PA658802182
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 525682
ClinVar RCV Id: RCV000629867 RCV001181390
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Gln657Pro
CA346750601
NM_000179.3:c.1970A>C