Canonical Allele Identifier: PA645414687
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 228918
ClinVar RCV Id: RCV000221769 RCV000232140
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala226Val
CA10576963
NM_000257.4:c.677C>T