Canonical Allele Identifier: PA645383693
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 419599
ClinVar RCV Id: RCV000479350 RCV001037784 RCV001019454
ClinVar Variation Id: 632908
ClinVar RCV Id: RCV000780482 RCV001525394
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Thr1085Ser
CA070494
NM_000179.3:c.3254C>G
CA1649450
NM_000179.3:c.3253A>T