Canonical Allele Identifier: PA658749571
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 491954
ClinVar RCV Id: RCV000584693 RCV000587024 RCV000629874 RCV000610333 RCV004002353
ClinVar Variation Id: 2008580
ClinVar RCV Id: RCV002828723
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Met1202Leu
CA346760557
NM_000179.3:c.3604A>C
CA346760558
NM_000179.3:c.3604A>T