Canonical Allele Identifier: PA132036
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43039
ClinVar RCV Id: RCV000201450 RCV000035933 RCV000475488 RCV000627158 RCV000852453 RCV000619414 RCV000766463 RCV000769443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Arg1606His
CA015352
NM_000257.4:c.4817G>A