Canonical Allele Identifier: PA180867
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 177851
ClinVar RCV Id: RCV000154488 RCV000628879 RCV000989189 RCV001183972 RCV001560656 RCV002321636
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1051Val
CA013389
NM_000257.4:c.3152C>T