Canonical Allele Identifier: PA2827628561
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 524356
ClinVar RCV Id: RCV000628087 RCV001189988
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gln65His
CA382521184
NM_001351834.2:c.195G>C
CA382521185
NM_001351834.2:c.195G>T