Canonical Allele Identifier: PA098066
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43005
ClinVar RCV Id: RCV000035899 RCV000629028 RCV000417392 RCV000589082 RCV000790631 RCV000758069
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu1426Lys
CA014743
NM_000257.4:c.4276G>A