Canonical Allele Identifier: PA2826625832
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 41587
ClinVar RCV Id: RCV000034491 RCV000217580 RCV000231596
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268421.1:p.Ile334Phe
CA008568
NM_001281492.2:c.1000A>T