Canonical Allele Identifier: PA645378170
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 419112
ClinVar RCV Id: RCV000482378 RCV000537973 RCV000565704 RCV003387854 RCV004002285
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Ala23Pro
CA16617616
NM_000179.3:c.67G>C