Canonical Allele Identifier: PA2826636178
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 581776
ClinVar RCV Id: RCV000705699 RCV002442532
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001268423.1:p.Ser504Phe
CA346754006
NM_001281494.2:c.1511C>T