Allele Registry

Canonical Allele Identifier: PA2826627072

Gene: MSH6 HGNC NCBI

ClinVar RCV:

RCV000160679

RCV000772630

RCV000821022

RCV003998496

ClinVar Variation:

182634

HGVS (amino-acid)	Matching Registered Transcripts
NP_001268421.1:p.Thr624Pro	CA009921 NM_001281492.2:c.1870A>C