Canonical Allele Identifier: PA131712
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 42818
ClinVar RCV Id: RCV000035694 RCV000201479 RCV000195997
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Val338Ala
CA010070
NM_000257.4:c.1013T>C