Canonical Allele Identifier: PA2826634292
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 823398
ClinVar RCV Id: RCV001019618 RCV001860952 RCV003467653 RCV003238829
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Thr21Asn
CA346740929
NM_001281494.2:c.62C>A