Canonical Allele Identifier: PA097861
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 372428
ClinVar RCV Id: RCV000414445 RCV003586178
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asn187Lys
CA16042879
NM_000257.4:c.561C>G
CA389052546
NM_000257.4:c.561C>A