Canonical Allele Identifier: PA298143
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 181919
ClinVar RCV Id: RCV000159684 RCV000219319 RCV000532840
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000042.3:p.Met557Ile
CA298141
NM_000051.4:c.1671G>A
CA382535115
NM_000051.4:c.1671G>C
CA382535116
NM_000051.4:c.1671G>T