Canonical Allele Identifier: PA2499230362
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1035824

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ile1671Met
CA044755
NM_000257.4:c.5013C>G