Canonical Allele Identifier: PA2573165079
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 1677914
ClinVar RCV Id: RCV002224505 RCV003375608 RCV003586319 RCV004005541
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Glu894Asp
CA389047395
NM_000257.4:c.2682A>C
CA389047397
NM_000257.4:c.2682A>T