Canonical Allele Identifier: PA098568
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 2736089
ClinVar RCV Id: RCV003587423
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Leu390Val
CA389051200
NM_000257.4:c.1168C>G
CA2695219143
NM_000257.4:c.1168_1170delinsGTT