Canonical Allele Identifier: PA180722
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 177763
ClinVar RCV Id: RCV000487427 RCV000795089 RCV001699209 RCV002426736 RCV003486688 RCV004532744
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala893Val
CA012811
NM_000257.4:c.2678C>T