Canonical Allele Identifier: PA2825111762
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1721088
ClinVar RCV Id: RCV002294800
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Asn897Lys
CA389047366
NM_000257.4:c.2691C>G
CA389047367
NM_000257.4:c.2691C>A