Canonical Allele Identifier: PA357564
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 220943
ClinVar RCV Id: RCV000205455 RCV000217289 RCV000519500 RCV001711360 RCV003997660
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Asn1327Ser
CA072431
NM_000179.3:c.3980A>G