Canonical Allele Identifier: PA2499230397
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1172002
ClinVar RCV Id: RCV001525582
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val1044Leu
CA389045435
NM_000257.4:c.3130G>T
CA389045437
NM_000257.4:c.3130G>C