Canonical Allele Identifier: PA296694
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 181270
ClinVar RCV Id: RCV000158681 RCV000687792 RCV001176076 RCV001290657 RCV002336359
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1677Cys
CA015584
NM_000257.4:c.5029C>T