Canonical Allele Identifier: PA098388
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 14098
ClinVar RCV Id: RCV000015154 RCV000158522 RCV000472342 RCV000621362 RCV001170499 RCV002490371
ClinVar Variation Id: 42890
ClinVar RCV Id: RCV000158521 RCV000243586 RCV000461730 RCV001170500 RCV004534738
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gly741Arg
CA012004
NM_000257.4:c.2221G>A
CA012013
NM_000257.4:c.2221G>C