Canonical Allele Identifier: PA151472
Gene: MSH6 HGNC NCBI

Linked Data

ClinVar Variation Id: 89552
ClinVar RCV Id: RCV000115440 RCV000121575 RCV000659887 RCV000588752 RCV001353587 RCV001083709 RCV001564013 RCV001798257 RCV003492405
ClinVar Variation Id: 921162
ClinVar RCV Id: RCV001180419 RCV002560801
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000170.1:p.Glu221Asp
CA016186
NM_000179.3:c.663A>C
CA346739374
NM_000179.3:c.663A>T