Canonical Allele Identifier: PA658680170
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 483841
ClinVar RCV Id: RCV000565483 RCV000758664 RCV001858309
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala159Thr
CA346738592
NM_000179.3:c.475G>A