Canonical Allele Identifier: PA181012
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 177924
ClinVar RCV Id: RCV000154584 RCV001184478
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Gln914His
CA012994
NM_000257.4:c.2742G>T
CA389047206
NM_000257.4:c.2742G>C