Canonical Allele Identifier: PA913192080
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 630179
ClinVar RCV Id: RCV000775313 RCV000799448 RCV004001442
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Met303Thr
CA346740714
NM_000179.3:c.908T>C