Canonical Allele Identifier: PA658680621
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483792
ClinVar RCV Id: RCV000570527 RCV000816280 RCV003465239 RCV004530607
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala494Val
CA346746046
NM_000179.3:c.1481C>T