Canonical Allele Identifier: PA2825109829
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 3072888
ClinVar RCV Id: RCV004014902
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Met439Ile
CA389050873
NM_000257.4:c.1317G>T
CA389050874
NM_000257.4:c.1317G>A
CA389050875
NM_000257.4:c.1317G>C